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311343-00-7

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311343-00-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 311343-00-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,1,3,4 and 3 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 311343-00:
(8*3)+(7*1)+(6*1)+(5*3)+(4*4)+(3*3)+(2*0)+(1*0)=77
77 % 10 = 7
So 311343-00-7 is a valid CAS Registry Number.

311343-00-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(N-acetyl-S-trityl-L-cysteinyl)-S-acetylcysteamine

1.2 Other means of identification

Product number -
Other names N-(N-acetyl-S-trityl-L-cysteinyl)-S-acetylcyste-amine

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:311343-00-7 SDS

311343-00-7Downstream Products

311343-00-7Relevant articles and documents

NAC/MEA conjugate: A new potent antioxidant which increases the GSH level in various cell lines

Oiry, Joel,Mialocq, Patricia,Puy, Jean Y.,Fretier, Philippe,Clayette, Pascal,Dormont, Dominique,Imbach, Jean L.

, p. 1189 - 1191 (2001)

I-152 is a prodrug of NAC and MEA with potent pro-GSH effects in human macrophages, astrocytes and lymphocytes. This molecule could be of interest in HIV infection in respect to its antioxidant and anti-HIV activities, but also in other diseases to counte

Novel antioxidants, preparation processes and their uses

-

Page 12, (2010/02/08)

The invention concerns a process for preparing compounds of general formula (I) wherein R and R′ represent an alkyl radical or an aryl group; and R″ is hydrogen or a CO—R1 group wherein R1 is an alkyl radical or an aryl group; and wherein these compounds are or not in the thiazolidine form; by protecting the N-acyl-L-cysteine to form an intermediate compound; and then by coupling said intermediate compound with S-acylcysteamine hydrochloride or with thiazolidine.

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