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90741-27-8

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90741-27-8 Usage

General Description

(S)-tert-butyl 1-benzyl-5-oxopyrrolidine-2-carboxylate is a chemical substance with a specific stereochemistry, implied by the (S) prefix. It belongs to a class of compounds known as pyrrolidines, which are four-membered heterocyclic compounds containing a nitrogen atom. This chemical has two functional groups, a carboxylate group and a benzyl group. The carboxylate group is attached to a tertiary butyl (tert-butyl) group, a type of alkyl group. The benzyl group gives the molecule its aromatic property. Although there is no specific information about its uses, compounds in this class often serve as intermediates in the synthesis of other chemicals, in pharmaceuticals, or in material science.

Check Digit Verification of cas no

The CAS Registry Mumber 90741-27-8 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, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 90741-27:
(7*9)+(6*0)+(5*7)+(4*4)+(3*1)+(2*2)+(1*7)=128
128 % 10 = 8
So 90741-27-8 is a valid CAS Registry Number.

90741-27-8SDS

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 (S)-tert-Butyl 1-benzyl-5-oxopyrrolidine-2-carboxylate

1.2 Other means of identification

Product number -
Other names tert-butyl (2S)-1-benzyl-5-oxopyrrolidine-2-carboxylate

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:90741-27-8 SDS

90741-27-8Downstream Products

90741-27-8Relevant articles and documents

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

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Paragraph 0053; 0054; 0056, (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 beta-turn based on the GLDV motif of cell adhesion proteins

Davies, David E.,Doyle, Paul M.,Hill, Richard D.,Young, Douglas W.

, p. 301 - 312 (2007/10/03)

The (3S,6S,10S)-7/5 bicyclic lactam 8, designed as an external turn constraint, was synthesised by a new stereoselective route involving Eschenmoser condensation. The cyclic peptide 35 containing the integrin recognition motif GLDV added across the amino

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,

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