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Carbamic acid, [1-(phenylmethyl)-2-(1-pyrrolidinyl)-2-thioxoethyl]-, 1,1-dimethylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88815-92-3

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88815-92-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88815-92-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,8,1 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 88815-92:
(7*8)+(6*8)+(5*8)+(4*1)+(3*5)+(2*9)+(1*2)=183
183 % 10 = 3
So 88815-92-3 is a valid CAS Registry Number.

88815-92-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(thio-t-Boc-α-aminophenylalanyl)-azacyclopentane

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:88815-92-3 SDS

88815-92-3Relevant academic research and scientific papers

In Situ Reagent for Thionation of Amides, Peptides and Lactams

Brillon, Denis

, p. 3085 - 3095 (2007/10/02)

An in situ reagent 1A for thionation of amides, peptides and lactams is prepared from phosphorus decasulfide/sodium carbonate (1:1 ratio) in THF at 25 deg C.

FACILE REGIOSELECTIVE FORMATION OF THIOPEPTIDE LINKAGES FROM OLIGOPEPTIDES WITH NEW THIONATION REAGENTS

Lajoie, G.,Lepine, F.,Maziak, L.,Belleau, B.

, p. 3815 - 3818 (2007/10/02)

The thionation reagent 1 and the new more soluble and readily purified analogue 2 permit, in appropriate solvents, the low temperature backbone thionation of oligopeptides in a regioselective manner and in high yields.

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