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Acetic acid, [(1-methylethyl)thio][[(phenylmethoxy)carbonyl]amino]-, 1,1-dimethylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

446271-42-7

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446271-42-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 446271-42-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,6,2,7 and 1 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 446271-42:
(8*4)+(7*4)+(6*6)+(5*2)+(4*7)+(3*1)+(2*4)+(1*2)=147
147 % 10 = 7
So 446271-42-7 is a valid CAS Registry Number.

446271-42-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[N-(benzyloxycarbonyl)amino]-2-(isopropylthio)acetic acid tert-butyl ester

1.2 Other means of identification

Product number -
Other names Benzyloxycarbonylamino-isopropylsulfanyl-acetic acid tert-butyl ester

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:446271-42-7 SDS

446271-42-7Downstream Products

446271-42-7Relevant academic research and scientific papers

Toward synthesis of alpha-alkyl amino glycines (A3G), new amino acid surrogates.

Yaouancq, Loic,Rene, Loic,Tran Huu Dau, Marie-Elise,Badet, Bernard

, p. 5408 - 5411 (2007/10/03)

A general method giving access to protected alpha-alkyl amino glycines (A3G) 4 from the previously described precursor alpha-isopropylthioglycine 1 is described. In the presence of N-bromosuccinimide, displacement of the thiol by a large variety of amines afforded the corresponding racemic amino acid mimics. The efficiency of the reaction was strongly dependent on the protective groups of the nucleophile used in the condensation.

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