| CAS number | Product name | Information |
|---|
| 133565-45-4
| Fmoc-L-Aspartimol(otbu) | order / more information... |
| 205598-51-2 | H-D-Lys-NH2 . 2 HCl | IUPAC Name H-D-Lys-NH2 . 2 HCl
CAS Number 205598-51-2
Chemical Formula C6H17Cl2N3O
Synonyms: H-D-Lys-NH2;H-D-LYS-NH2 2 HCL;D-LYSINE-NH2 2 HCL;D-LYSINE AMIDE DIHYDROCHLORIDE;D-LYSINE ALPHA-AMIDE DIHYDROCHLORIDE order / more information... |
| 175203-78-8
| 5-Chlorobenzofurazan-4-sulfonyl chloride | order / more information... |
| 643-79-8
| O-phthalic dicarboxaldehyde | order / more information... |
| 93983-66-5 | Dimethylhexanoic acid, cerium salt | IUPAC Name Dimethylhexanoic acid, cerium salt
CAS Number 93983-66-5
Chemical Formula C8H16 O2 . x Ce
Synonyms: dimethylhexanoic acid, cerium salt order / more information... |
| 268547-51-9 | 3-(2,4-Dichlorophenyl)-1h-pyrazol-4-amine | IUPAC Name 3-(2,4-Dichlorophenyl)-1h-pyrazol-4-amine
CAS Number 268547-51-9
Chemical Formula C9H7Cl2N3 order / more information... |
| 22205-45-4 | Copper(I) sulfide | http://en.wikipedia.org/wiki/Copper%28I%29_sulfide
IUPAC Name copper; copper(+1) cation; sulfanide
CAS Number 22891-51-6
Chemical Formula Cu2HS
Synonyms: 1308-78-7, 155903-69-8, 22205-45-4, 22891-51-6, Copper sulfide (Cu2S), Copper(I) sulfide, Cuprasulfide, CUPROUS SULFIDE, Cuprous sulfide (Cu2S), Dicopper monosulfide, Dicopper sulfide, Dicopper sulphide, EINECS 244-842-9 order / more information... |
| 23018-09-9
| Z-Tyr-Ala-OH | order / more information... |
| 64328-55-8
| 4-Ethylbenzohydrazide | order / more information... |
| 626-01-7
| 3-Iodoaniline | order / more information... |
| 111686-79-4 | Remacemide hydrochloride | IUPAC Name 2-amino-N-(1,2-diphenylpropan-2-yl)acetamide hydrochloride
CAS Number 111686-79-4
Chemical Formula C17H21ClN2O
Synonyms: 111686-79-4, 2-amino-N-(1,2-diphenylpropan-2-yl)acetamide hydrochloride, 2-amino-N-(1-methyl-1,2-diphenyl-ethyl)acetamide hydrochloride, (+-)-2-Amino-N-(1-methyl-1,2-diphenylethyl)acetamide monohydrochloride, 2-azanyl-N-(1,2-diphenylpropan-2-yl)ethanamide hydrochloride, Acetamide, 2-amino-N-(1-methyl-1,2-diphenylethyl)-, (+/-)- [CAS], Acetamide, 2-amino-N-(1-methyl-1,2-diphenylethyl)-, monohydrochloride,
(+-)-, C17H20N2O.HCl, C17H21ClN2O, CID60510, CPD000466281, D05714, FPL 12924AA, FPL-12924AA, LS-8063, MLS000758316, MLS001424175, PR-1032-644 [(+)-isomer], PR-1032-646 [(-)-isomer], PR 934-423A, PR-934-423A, REMACEMIDE HYDROCHLORIDE, Remacemide hydrochloride (USAN), Remacemide hydrochloride [USAN], remacemide monohydrochloride, (+-)-isomer, SAM001247078, SMR000466281 order / more information... |
| 2414-98-4 | Magnesium ethylate | IUPAC Name magnesium ethanolate
CAS Number 2414-98-4
Chemical Formula C4H10MgO2
Synonyms: 2414-98-4, C4H10MgO2, EINECS 219-323-5, Ethanol, magnesium salt, magnesium ethanolate, Magnesium ethoxide, Magnesium ethylate
Product info: Alkoxide (also called alcoholate ) is the conjugate bases of corresponding alcohol. They contain negatively charged oxygen atom, found as intermediaries in various reactions. Alkoxide is a strong reducing agent. The term alkoxide is for a compound formed from alcohol by replacing the hydrogen of the hydroxy group by a monovalent metal. Metal alkoxides are versatile reagents favoring the chemical reaction of condensation, esterification, alkoxylation and etherification, Claisen condensation, Wolf-Kishner reduction and Stobbe reaction are examples. They are used in wide range of applications in organic synthesis; Agrochemicals; Pharmaceuticals, colorants and aroma chemicals. They are used in manufacturing detergents and biodiesel. They also act as catalysts in polymerization and isomerizations.
Alkylation
Base catalyzed reaction
Cleaning
Condensation
Dehalogenenation
Deprotonations
Elimination reaction
Enolate formation
Isomerization reaction
Polymer application
Selective metalation
Super base application
Transesterfication
Inorganic superbases are typically salts with highly charged, small negative ions, e.g. lithium nitride, which has extreme negative charge density and so is highly attracted to acids, like the aqueous hydronium ion. Alkali and earth alkali metal hydrides (sodium hydride, calcium hydride) are superbases.
The base strength can be varied with choice of solvent and the structure of the alcohol. In the dimethyl sulfoxide (DMSO), the ion aggregates are solvated thus increasing the basicity. Alkyl groups in steric bulk of the tertiary alcohol make the alcoholate a stronger base compared to primary alcoholates and hydroxides and influence the speed, selectivity, and specificity. Generally primary alcoholate is soluble in the alcohol from which they are derived only. But sec-, and tert- alcoholates are soluble in ethers. Furthermore tert- alcoholates have high solubility in the hydrocarbons. In organic synthesis, higher solubility of tertiary alcoholates can generate " Schlosser base (or Lochmann-Schlosser base)" in combination with an alkyl lithium to. The Schlosser base is a commonly used superbase. Butyllithium exists as four-, or six-membered clusters, which are kinetically slow to react. The tertiary alcoholate (butoxide) serves to complex the lithium ion, which breaks the butyllithium clusters. This makes the butyllithium kinetically more reactive. Other such systems are collectively called harpoon bases. order / more information... |
| 3-(ethoxycarbonyl)-5-methyl-1-[4-(methylthio)phenyl]-4,5-dihydro-1H-pyrazole-5-carboxylic acid | order / more information... |
| 16652-71-4 | (2S)-pyrrolidine-2-carboxylic acid tert-butyl ester hydrochloride | IUPAC Name tert-butyl (2S)-pyrrolidine-2-carboxylate hydrochloride
CAS Number 5497-76-7
Chemical Formula C9H18ClNO2
Synonyms: (2S)-pyrrolidine-2-carboxylic acid tert-butyl ester hydrochloride, 5497-76-7, C9H18ClNO2, CID6453107, EINECS 226-835-2, tert-butyl (2S)-pyrrolidine-2-carboxylate hydrochloride, tert-Butyl L-prolinate hydrochloride order / more information... |
| 610-22-0 | Dimethyl 4-nitrophthalate | IUPAC Name:dimethyl 4-nitrobenzene-1,2-dicarboxylate
CAS Number:610-22-0
Chemical Formula:C10H9NO6
Synonyms: 1,2-Benzenedicarboxylic acid, 4-nitro-, dimethyl ester, 367486_ALDRICH, 4-nitrobenzene-1,2-dicarboxylic acid dimethyl ester, 4-nitrophthalic acid dimethyl ester, 610-22-0, 73784_FLUKA, AI3-09347, C10H9NO6, dimethyl 4-nitrobenzene-1,2-dicarboxylate, Dimethyl 4-nitrophthalate, Dimethyl-4-nitrophthalate, EINECS 210-212-7, NSC9410, NSC 9410, Phthalic acid, 4-nitro-, dimethyl ester, ST5319562, ZINC00499735 order / more information... |
| 544-62-7 | 3-stearyloxypropane-1,2-diol | IUPAC Name: 3-octadecoxypropane-1,2-diol
CAS Number: 544-62-7
Chemical Formula: C21H44O3
Synonyms: 01503944_BATYL, 10438-95-6, 1,2-Propanediol, 3-(octadecyloxy)-, 1-(Octadecyloxy)-2,3-dihydroxypropane, 1-O-Octadecylglycerol, 1-O-Octadecyl-rac-glycerol, 1-O-Octadecyl-sn-glycerol, 3-octadecoxypropane-1,2-diol, 3-(Octadecyloxy)-1,2-propanediol, 3-stearyloxypropane-1,2-diol, 4-01-00-02758 (Beilstein Handbook Reference), 544-62-7, 68990-53-4, AI3-18451, AIDS027321, AIDS-027321, .alpha.-Octadecylether of glycerol, alpha-Octadecylether of glycerol, B402_ALDRICH, Batilol, Batilol [INN], Batilolum [INN-Latin], (+)-Batylalcohol, BATYL ALCOHOL, BRN 1725677, BSPBio_002296, C13858, C18:0 Glyceryl 1-ether, C21H44O3, DivK1c_001035, DL-3-Octadecyloxy-1,2-propanediol, dl-Batyl alcohol, DL-Batylalcohol, EINECS 208-874-7, Glycerides, C14-22 mono-, Glycerine 1-monostearyl ether, Glycerol 1-octadecyl ether, Glycerol monooctadecyl ether, Glycerol octadecyl ether, Glyceryl-1-octadecyl ether, IDI1_001035, KBio1_001035, KBio2_002138, KBio2_004706, KBio2_007274, KBio3_001516, KBioGR_002296, KBioSS_002138, LS-120693, Monooctadecyl ether of glycerol, NCGC00095748-01, NCGC00095748-02, NCI60_002329, NINDS_001035, NSC284200, NSC 284200, NSC8716, rac- 1-O-N-Octadecyl glycerol, rac-Glycerol 1-octadecyl ether, SDCCGMLS-0066743.P001, SPBio_001617, Spectrum_001658, SPECTRUM1503983, Spectrum2_001609, Spectrum3_000738, Spectrum4_001778, Spectrum5_000395, Stearyl monoglyceride, WLN: Q1YQ1O18 order / more information... |
| 60307-25-7 | (±)-1-Methyl-5-oxopyrrolidine-2-acetic acid | IUPAC Name 2-(1-methyl-5-oxopyrrolidin-2-yl)acetic acid
CAS Number 60307-25-7
Chemical Formula C7H11NO3
Synonyms: (1)-1-Methyl-5-oxopyrrolidine-2-acetic acid, 2-(1-methyl-5-oxo-pyrrolidin-2-yl)acetic acid, 2-(1-methyl-5-oxopyrrolidin-2-yl)acetic acid, 2-(1-methyl-5-oxo-pyrrolidin-2-yl)ethanoic acid, 2-(5-keto-1-methyl-pyrrolidin-2-yl)acetic acid, 60307-25-7, C7H11NO3, EINECS 262-154-7, ZERO/009776 order / more information... |
| Vinyls | order / more information... |
| 193150-14-0 | (R)-3-(1-Tert-butoxycarbonylamino-ethyl)-benzoic acid | IUPAC Name Not available
CAS Number 193150-14-0
Chemical Formula Not available order / more information... |
| 50-56-6 | Oxytocin | IUPAC Name: 1-[16-amino-4-(2-amino-2-oxoethyl)-7-(3-amino-3-oxopropyl)-10-butan-2-yl-13-[(4-hydroxyphenyl)methyl]-3,6,9,12,15-pentaoxo-18,19-dithia-2,5,8,11,14-pentazacycloicosane-1-carbonyl]-N-[1-[(2-amino-2-oxoethyl)amino]-4-methyl-1-oxopentan-2-yl]pyrrolidine-2-carboxamide
CAS Number: 50-56-6
Chemical Formula: C43H66N12O12S2
Synonyms: 112457-76-8, 1-[16-amino-4-(2-amino-2-keto-ethyl)-7-(3-amino-3-keto-propyl)-13-(4-hydroxybenzyl)-3,6,9,12,15-pentaketo-10-sec-butyl-18,19-dithia-2,5,8,11,14-pentazacycloicosane-1-carbonyl]-N-[1-[(2-amino-2-keto-ethyl)carbamoyl]-3-methyl-butyl]pyrrolidine-2-carboxamide, 1-[16-amino-4-(2-amino-2-oxoethyl)-7-(3-amino-3-oxopropyl)-10-butan-2-yl-13-[(4-hydroxyphenyl)methyl]-3,6,9,12,15-pentaoxo-18,19-dithia-2,5,8,11,14-pentazacycloicosane-1-carbonyl]-N-[1-[(2-amino-2-oxoethyl)amino]-4-methyl-1-oxopentan-2-yl]pyrrolidine-2-carboxamide, 1-[16-amino-4-(2-amino-2-oxo-ethyl)-7-(3-amino-3-oxo-propyl)-13-[(4-hydroxyphenyl)methyl]-3,6,9,12,15-pentaoxo-10-sec-butyl-18,19-dithia-2,5,8,11,14-pentazacycloicosane-1-carbonyl]-N-[1-[(2-amino-2-oxo-ethyl)carbamoyl]-3-methyl-butyl]pyrrolidine-2-carboxamide, 1-[[16-azanyl-4-(2-azanyl-2-oxo-ethyl)-7-(3-azanyl-3-oxo-propyl)-10-butan-2-yl-13-[(4-hydroxyphenyl)methyl]-3,6,9,12,15-pentaoxo-18,19-dithia-2,5,8,11,14-pentazacycloicos-1-yl]carbonyl]-N-[1-[(2-azanyl-2-oxo-ethyl)amino]-4-methyl-1-oxo-pentan-2-yl]pyrrolidine-2-carboxamide, (1-Hemicystine)oxytocin, 3-Isoleucine-8-leucine vasopressin, 50-56-6, alpha-Hypophamine, Atonin O, BRN 3586108, C43H66N12O12S2, C4H10, Di-sipidin, EINECS 200-048-4, Endopituitrina, HSDB 2182, L-Cysteinyl-L-tyrosyl-L-isoleucyl-L-glutaminyl-L-asparaginyl-L-cysteinyl-L-prolyl-L-leucylglycinamide cyclic (1-6)-disulfide, LS-101130, NCGC00166145-01, NCGC00166145-02, Nobitocin S, O6379_SIGMA, Ocytocin, Ocytocinum, Orasthin, Ossitocina [DCIT], Oxetakain [Czech], Oxitocina [INN-Spanish], Oxystin, OXYTOCIN, OXYTOCIN 10 USP UNITS IN DEXTROSE 5%, OXYTOCIN 20 USP UNITS IN DEXTROSE 5%, OXYTOCIN 5 USP UNITS IN DEXTROSE 5%, Oxytocin acetate salt hydrate, Oxytocine [INN-French], Oxytocinum [INN-Latin], Oxytocin [USAN:BAN:INN:JAN], Oxytocin [USAN:INN:BAN:JAN], Partocon, Pitocin, Piton S, Posterior pituitary extract, Presoxin, SMP2_000176, Synpitan, Synthetic oxytocin, Syntocin, Syntocinon, Syntocinone, Utedrin, Uteracon, Vasopressin, 3-L-isoleucine-8-L-leucine-
Product info: Oxytocin is a hormone that helps relax and reduce blood pressure and cortisol levels. Oxytocin increases pain thresholds, has anti anxiety effects, and stimulates various types of positive social interaction. In addition, oxytocin promotes growth and healing. The nonapeptide oxytocin, originally known to stimulate labor and milk ejection, appears to play an important role stress and pain. Oxytocin can induce anti-stress-like effects such as reduction of blood pressure and cortisol levels. It increases pain thresholds, exerts an anxiolytic-like effect and stimulates various types of positive social interaction. In addition, it promotes growth and healing. Repeated exposure to oxytocin causes long-lasting effects by influencing the activity of other transmitter systems, a pattern which makes oxytocin potentially clinically relevant. Oxytocin can be released by various types of non-noxious sensory stimulation, for example by touch and warmth. Ingestion of food triggers oxytocin release by activation of vagal afferents. Most likely, oxytocin can also be released by stimulation of other senses such as olfaction, as well as by certain types of sound and light. In addition, purely psychological mechanisms may trigger the release of oxytocin. This means that positive interaction involving touch and psychological support may be health-promoting. The social interaction of daily life, as well as a positive environment, continuously activate this system. In addition, various types of psychotherapy involving transfer of support, warmth and empathy are likely to induce similar effects, which thus contribute to the positive effects of these kinds of therapies. (http://www.raysahelian.com/)
Oxytocin in a nine amino acid peptide that is synthesized in hypothalamic neurons and transported down axons of the posterior pituitary for secretion into blood. Oxytocin is also secreted within the brain and from a few other tissues, including the ovaries and testes. Oxytocin differs from antidiuretic hormone in two of the nine amino acids. Both hormones are packaged into granules and secreted along with carrier proteins called neurophysins. (http://www.vivo.colostate.edu/)
Oxytocin, derived from the Greek words oxus, meaning sharp, and tokos, meaning childbirth, is a peptide hormone consisting of nine amino acids (Mitchell et al, 1998, Engstrom, 2002). The amino acids are: NH2 – Gly – Leu – Pro – Cys – Asn – Gln – Ile – Tyr – Cys, with a disulfide linkage between the two Cys residues (Messer, 2000). This hormone, to date, is the most potent stimulant of uterine contractions in mammals, and is administered in the clinical setting to induce labor (Serradeil-Le Gal et al, 2004). Oxytocin is produced in the paraventricular and supraoptical nuclei of the hypothalamus, and stored in the posterior pituitary gland (Engstrom, 2002). Cervical distension within the uterus causes an action potential to travel to the hypothalamus, signaling the production and release of oxytocin (Blanks et al, 2003). During pregnancy, the quantity of oxytocin produced by the hypothalamus increases by roughly 50% (Russell et al, 1998, Blanks et al, 2003). Once in circulation, it travels through the blood to its target site. Oxytocin has a half-life of 5-15 minutes in circulation, after which it is degraded in the liver by oxytocinase (Engstrom, 2002). In addition, oxytocin is synthesized locally within the epithelium of the uterus (endometrium) (Blanks et al, 2003). Local and hypothalamic oxytocin leads to myometrial contractions, which ultimately leads to the expulsion of the young (parturition) (Russell et al, 1998, Blanks et al, 2003). (http://web.sau.edu/) order / more information... |
| 465515-31-5 | 5-Boronothiophene-2-carboxylic acid | IUPAC Name: 5-boronothiophene-2-carboxylic acid
CAS Number: Not Available
Chemical Formula: C5H5BO4S
Synonyms: 5-borono-2-thenoic acid, 5-boronothiophene-2-carboxylic acid, 5-(dihydroxyboranyl)thiophene-2-carboxylic acid, 5-(dihydroxyboryl)thiophene-2-carboxylic acid, AF-399/25053010, C5H5BO4S, CID2779807, MO 00596 order / more information... |
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| Sponge Nickel Catalyst A-5001 | order / more information... |
| 98049-69-5
| Lipoxin B4 | order / more information... |
| 87130-20-9 | Diethofencarb | IUPAC Name: propan-2-yl N-(3,4-diethoxyphenyl)carbamate
CAS Number: 87130-20-9
Chemical Formula: C14H21NO4
Synonyms: 1-Methylethyl (3,4-diethoxyphenyl)carbamate, 34087_RIEDEL, 3,4-Diethoxycarbanilate d'isopropyle [French], 3,4-Dietossicarbanilato di isopropile [Italian], 3,4-Dietoxicarbanilato de isopropilo [Portuguese], 3,4-Dietoxicarbanilato de isopropilo [Spanish], 87130-20-9, C11077, C14H21NO4, Carbamic acid, (3,4-diethoxyphenyl)-, 1-methylethyl ester, Diethofencarb, Diethofencarb [ISO], EE4038703, Isopropyl-3,4-diethoxycarbanilaat [Dutch], Isopropyl-3,4-diethoxycarbanilat [Danish], Isopropyl 3,4-diethoxycarbanilate, Isopropyl-3,4-diethoxycarbanilat [German], Isopropyl 3,4-diethoxyphenylcarbamate, isopropyl N-(3,4-diethoxyphenyl)carbamate, LS-49258, N-(3,4-diethoxyphenyl)carbamic acid isopropyl ester, NCGC00163730-01, Powmyl WP, propan-2-yl N-(3,4-diethoxyphenyl)carbamate, S-1605, S-165, S 32165 order / more information... |
| 161796-78-7 | Esomeprazole | http://en.wikipedia.org/wiki/Esomeprazole
IUPAC Name: sodium 5-methoxy-2-[(4-methoxy-3,5-dimethylpyridin-2-yl)methylsulfinyl]benzimidazol-1-ide
CAS Number: 95510-70-6
Chemical Formula: C17H18N3NaO3S
Synonyms: 161796-78-7, 1H-Benzimidazole, 5-methoxy-2-(((4-methoxy-3,5-dimethyl-2-pyridinyl)methyl)sulfinyl)-, sodium salt, 5-Methoxy-2-(((4-methoxy-3,5-dimethyl-2-pyridyl)methyl)sulfinyl)benzimidazole, sodium salt, 95510-70-6, Andra, C17H18N3NaO3S, D01207, D04056, Esomeprazole Sodium, Esomeprazole sodium (USAN), H 168/68 sodium, Losec Sodium, Losec sodium (TN), LS-33032, Nexium IV, Nexium IV (TN), OMEPRAZOLE SODIUM, Omeprazole sodium (USAN), Omeprazole sodium [USAN], sodium 5-methoxy-2-[(4-methoxy-3,5-dimethyl-2-pyridyl)methylsulfinyl]benzimidazol-1-ide, sodium 5-methoxy-2-[(4-methoxy-3,5-dimethyl-pyridin-2-yl)methylsulfinyl]benzimidazol-1-ide, sodium 5-methoxy-2-[(4-methoxy-3,5-dimethylpyridin-2-yl)methylsulfinyl]benzimidazol-1-ide order / more information... |