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

72719-13-2

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72719-13-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72719-13-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,7,1 and 9 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 72719-13:
(7*7)+(6*2)+(5*7)+(4*1)+(3*9)+(2*1)+(1*3)=132
132 % 10 = 2
So 72719-13-2 is a valid CAS Registry Number.

72719-13-2SDS

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 methyl N-phenylacetylpyroglutamate

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:72719-13-2 SDS

72719-13-2Relevant academic research and scientific papers

Identification, Structure determination and Synthesis of Until now Unknown Amino Acid Conjugates from Human Urine I

Spiteller, Michael,Spiteller, Gerhard

, p. 249 - 258 (1980)

The conjugates of glycine with furan 2.5-dicarboxylic acid and of picolinic acid as well as a conjugate of pyroglutamic acid with phenylacetic acid, previously unknown as natural metabolites, were detected to be normal metabolites in human urine. - Keywords: Amino acid conjugates; Conjugates of amino acids; Metabolic profiling

Straightforward and facile approach toward the n-derivatization of pyroglutamates through mitsunobu reaction: Synthesis of N-alkyl/N-acyl pyroglutamates

Panday, Sharad Kumar,Prasad, Jagdish,Pathak, Manoher Bhushan

experimental part, p. 3654 - 3661 (2011/10/09)

Pyroglutamates have been acknowledged as useful chiral synthons for the synthesis of many bioactive natural products, ACE inhibitors, and conformationally constrained peptides. Though the reactivity differences between two differential carbonyl groups have been well exploited, there is still a dearth of publications on the N-alkylation/acylation of native pyroglutamate as such, due to the relatively low reactivity of NH of pyroglutamates. In the present communication, we report for the first time a simple and efficient methodology for the N-alkylation/acylation of pyroglutamate via Mitsunobu reaction. Copyright Taylor & Francis Group, LLC.

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