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L-Cysteine, N-acetyl-S-ethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

31386-36-4

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31386-36-4 Usage

Chemical Properties

White Solid

Check Digit Verification of cas no

The CAS Registry Mumber 31386-36-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,3,8 and 6 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 31386-36:
(7*3)+(6*1)+(5*3)+(4*8)+(3*6)+(2*3)+(1*6)=104
104 % 10 = 4
So 31386-36-4 is a valid CAS Registry Number.

31386-36-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R)-2-acetamido-3-ethylsulfanylpropanoic acid

1.2 Other means of identification

Product number -
Other names L-Cysteine,N-acetyl-S-ethyl

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:31386-36-4 SDS

31386-36-4Downstream Products

31386-36-4Relevant academic research and scientific papers

Carvacrol codrugs: A new approach in the antimicrobial plan

Cacciatore, Ivana,Di Giulio, Mara,Fornasari, Erika,Di Stefano, Antonio,Cerasa, Laura Serafina,Marinelli, Lisa,Turkez, Hasan,Di Campli, Emanuela,Di Bartolomeo, Soraya,Robuffo, Iole,Cellini, Luigina

, (2015/06/02)

Objective: The increasing prevalence of antibiotic-resistant bacterial infections led to identify alternative strategies for a novel therapeutic approach. In this study, we synthesized ten carvacrol codrugs - obtained linking the carvacrol hydroxyl group

An improved method for cysteine alkylation

Perrey, David A.,Uckun, Fatih M.

, p. 1859 - 1861 (2007/10/03)

An improved method for the synthesis of S-alkylated cysteine derivatives with branched alkyl chains is reported. These compounds can be obtained in good yield and high purity by refluxing the cysteine thiol with the appropriate alkyl bromide in a solution of sodium ethoxide in ethanol.

The S-alkyl chain length as a determinant of the anti-leukemic activity of cysteine chloromethyl ketone compounds

Perrey, David A.,Scannell, Michael P.,Narla, Rama Krishna,Uckun, Fatih M.

, p. 551 - 552 (2007/10/03)

A series of cysteine chloromethyl ketone compounds with a systematic variation of the S-alkyl chain length have been synthesized in order to gauge the effect of the alkyl chain length on the cytotoxicity of these compounds against human acute lymphoblastic leukemia cells. Comparable activities were observed for compounds with S-alkyl chains ranging from pentyl to dodecyl, with the best being undecyl (IC50 = 1.7 μM) and dodecyl (IC50 = 2.0 μM) against B-lineage leukemia cells and hexyl (IC50 = 0.7 μM) against T-lineage leukemia cells. (C) 2000 Elsevier Science Ltd. All rights reserved.

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