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L-Proline, 1-(phenylmethyl)-5-thioxo-, 1,1-dimethylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90741-31-4

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90741-31-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90741-31-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,7,4 and 1 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 90741-31:
(7*9)+(6*0)+(5*7)+(4*4)+(3*1)+(2*3)+(1*1)=124
124 % 10 = 4
So 90741-31-4 is a valid CAS Registry Number.

90741-31-4SDS

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 L-Proline, 1-(phenylmethyl)-5-thioxo-, 1,1-dimethylethyl ester

1.2 Other means of identification

Product number -
Other names -

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:90741-31-4 SDS

90741-31-4Relevant academic research and scientific papers

A the non-peptide class perishes weakly inhibiting protein antagonists and its synthetic method and application (by machine translation)

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Paragraph 0057; 0058; 0059, (2016/10/08)

This invention discloses a kind of the non-peptide class perishes weakly inhibiting protein antagonist and method for preparing the same and application, which aims to provide a better anticancer effect with the non-peptide class perishes weakly inhibitin

Synthesis of an external β-turn based on the GLDV motif of cell adhesion proteins

Davies, David E.,Doyle, Paul M.,Farrant, R. Duncan,Hill, Richard D.,Hitchcock, Peter B.,Sanderson, Paul N.,Young, Douglas W.

, p. 8887 - 8891 (2007/10/03)

The (3S,6S,10S)-7/5 bicyclic lactam 4, designed as an external turn constraint, was synthesised by a new stereoselective route involving Eschenmoser condensation. Calculated preferred conformations compare well with the preferred solid state conformation,

Angiotensin II antagonists

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, (2008/06/13)

This invention provides novel heterocyclic derivatives, their pharmaceutical formulations, and their use for antagonizing angiotensin II receptors in mammals.

Angiotensin II antagonist intermediates

-

, (2008/06/13)

This invention provides novel heterocyclic derivatives, their pharmaceutical formulations, and their use for antagonizing angiotensin II receptors in mammals.

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