ChemicalBook > Product Catalog >Biochemical Engineering >Amino Acids and Derivatives >Natural amino acids and derivatives >H-L-Cys(Trt)-NH2 HCl

H-L-Cys(Trt)-NH2 HCl

H-L-Cys(Trt)-NH2 HCl Suppliers list
Company Name: J & K SCIENTIFIC LTD.  
Tel: 18210857532 18210857532
Email: jkinfo@jkchemical.com
Company Name: Meryer (Shanghai) Chemical Technology Co., Ltd.  
Tel: 4006356688 18621169109
Email: market03@meryer.com
Company Name: Alfa Aesar  
Tel: 400-6106006
Email: saleschina@alfa-asia.com
Company Name: GL Biochem (Shanghai) Ltd  
Tel: 21-61263452 13641803416
Email: ymbetter@glbiochem.com
Company Name: Shanghai Hanhong Scientific Co.,Ltd.  
Tel: 021-54306202 13764082696
Email: info@hanhongsci.com

H-L-Cys(Trt)-NH2 HCl manufacturers

  • H-L-CYS(TRT)-NH2 HCL
  • H-L-CYS(TRT)-NH2 HCL pictures
  • $1.00
  • 2019-09-02
  • CAS:166737-85-5
  • Min. Order: 1KG
  • Purity: ≥98%
  • Supply Ability: 200kg
H-L-Cys(Trt)-NH2 HCl Basic information
Product Name:H-L-Cys(Trt)-NH2 HCl
Synonyms:S-TRITYL-L-CYSTEINE AMIDE HYDROCHLORIDE;H-Cys(Trt)-NH2;(2R)-2-amino-3-[(triphenylmethyl)sulfanyl]propanamide;S-Trityl-L-cysteinaMide, 98%;PropanaMide,2-aMino-3-[(triphenylMethyl)thio]-, (2R)-;H-L-Cys(Trt)-NH2;L-Cys(Trt)-NH2;S-Trityl-L-cysteine amide≥ 98% (HPLC)
CAS:166737-85-5
MF:C22H22N2OS
MW:362.49
EINECS:
Product Categories:Pharmaceutical Intermediates
Mol File:166737-85-5.mol
H-L-Cys(Trt)-NH2 HCl Structure
H-L-Cys(Trt)-NH2 HCl Chemical Properties
Boiling point 543.2±50.0 °C(Predicted)
density 1.203±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
pka15.83±0.50(Predicted)
form Powder
color Off-white
Safety Information
MSDS Information
H-L-Cys(Trt)-NH2 HCl Usage And Synthesis
Chemical PropertiesWhite to off-white powder
Uses(2R)-2-Amino-3-[(triphenylmethyl)thio]propanamide is a useful building block for organic synthesis.
Synthesis
202752-01-0

202752-01-0

H-L-CYS(TRT)-NH2 HCL

166737-85-5

General procedure for the synthesis of S-trityl-L-cysteamine from (9H-fluoren-9-yl)methyl (R)-(1-amino-1-oxo-3-(triphenylmethylthio)propan-2-yl)carbamate: (R)-(9H-fluoren-9-yl)methyl (1-amino-1-oxo-3-(triphenylmethylthio)propan-2-yl)carbamate (4 g. 6.84 mmol) was dissolved in N,N-dimethylformamide (20 mL), piperidine (0.14 mL, 1.368 mmol) was added and the reaction was carried out for 4 h at room temperature. The progress of the reaction was monitored by thin layer chromatography (TLC). Upon completion of the reaction, the reaction mixture was washed with saturated aqueous sodium chloride solution and subsequently extracted with dichloromethane. The organic phase was dried with anhydrous sodium sulfate, concentrated and purified by column chromatography (eluent: methanol/dichloromethane, 1%-5% gradient) to afford the title product S-trityl-L-cysteamine as a yellow oil (2.3 g, yield: 92%).

References[1] Patent: CN106432014, 2017, A. Location in patent: Paragraph 0079; 0083; 0084; 0085; 0119; 0123; 0124; 0125
[2] Patent: WO2008/116302, 2008, A1. Location in patent: Page/Page column 43-44
H-L-Cys(Trt)-NH2 HCl Preparation Products And Raw materials
Raw materialsL-Cysteine, S-(triphenylmethyl)-, methyl ester-->202752-01-0-->N,N-Dimethylformamide-->Piperidine
Tag:H-L-Cys(Trt)-NH2 HCl(166737-85-5) Related Product Information
L-Glutamine N-[S-Trityl-L-cysteinyl]glycine H-L-Cys(Trt)-OtBu*HCl S-Trityl-L-cysteine H-L-Cys(Trt)-NH2 HCl S-Trityl-D-cysteine