H-CYS(BZL)-OME HCL
H-CYS(BZL)-OME HCL Basic information
- Product Name:
- H-CYS(BZL)-OME HCL
- Synonyms:
-
- L-Cys(Bzl)-OMe·HCl
- BENZYL-L-CYSTEINE METHYL ESTER HYDROCHLORIDE
- H-CYS(BZL)-OME HCL
- CYSTEINE(BZL)-OME HCL
- S-BENZYL-L-CYSTEINE METHYL ESTER HYDROCHLORIDE
- S-BENZYL-L-CYSTEINE METHYL ESTER HYDROCHLORIDE SALT
- S-benzyl-L-cysteine methyl ester*hydrochloride cr
- methyl S-benzyl-L-cysteinate hydrochloride
- CAS:
- 16741-80-3
- MF:
- C11H16ClNO2S
- MW:
- 261.77
- EINECS:
- 240-803-5
- Product Categories:
-
- Amino Acids and Derivatives
- Amino Acid Derivatives
- Amino Acids
- Mol File:
- 16741-80-3.mol
H-CYS(BZL)-OME HCL Chemical Properties
- Melting point:
- 160-162 °C(Solv: methanol (67-56-1); ethyl ether (60-29-7))
- storage temp.
- Inert atmosphere,Store in freezer, under -20°C
- solubility
- Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
- form
- Powder
- color
- White to light yellow
- CAS DataBase Reference
- 16741-80-3(CAS DataBase Reference)
MSDS
- Language:English Provider:SigmaAldrich
H-CYS(BZL)-OME HCL Usage And Synthesis
Chemical Properties
Crystalline
Uses
S-Benzyl-L-cysteine Methyl Ester Hydrochloride is a potential amino acid antagonists in bacteria
Synthesis
67-56-1
3054-01-1
16741-80-3
The general procedure for the synthesis of S-benzyl-L-cysteine methyl ester hydrochloride from methanol and S-benzyl-L-cysteine is as follows: Example 1: Synthesis of OFN(L-cyanocyclopropyl)-3-phenylmethylsulfonyl-2(R)-(2,2,2-trifluoro-1(RS)-thiophen-2-yl-ethylamino)propionamide Step 1: 2(R)-amino-3-phenylmethane-based sulfuric acid (commercially available) (4.01 g, 19.0 mmol) was dissolved in methanol (100 mL), cooled to 0°C and stirred. HCl gas was passed into this solution for 15 min, after which the reaction mixture was sealed and stirring was continued overnight at room temperature. After completion of the reaction, the solvent was evaporated under vacuum to give propyl methyl 2(R)-amino-3-phenylmethane sulfate hydrochloride (4.98 g) in quantitative yield.
References
[1] Patent: WO2005/28429, 2005, A2. Location in patent: Page/Page column 64
[2] Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2006, vol. 45, # 8, p. 1942 - 1944
[3] European Journal of Medicinal Chemistry, 2012, vol. 55, p. 176 - 187,12
[4] Organic Preparations and Procedures International, 1991, vol. 23, # 1, p. 93 - 102
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H-CYS(BZL)-OME HCL(16741-80-3)Related Product Information
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- DL-Cysteine hydrochloride
- S-Methyl-L-cysteine
- H-CYS(BZL)-OME HCL
- L-Cysteine
- METHYL 2-AMINO-3-MERCAPTOPROPANOATE HYDROCHLORIDE
- S-BENZYL-L-CYSTEINOL
- S-METHYL-L-CYSTEINE METHYL ESTER HYDROCHLORIDE
- S-ETHYL-L-CYSTEINE
- H-D-CYS(BZL)-OH