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32221-83-3

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32221-83-3 Usage

Chemical Properties

White powder

Check Digit Verification of cas no

The CAS Registry Mumber 32221-83-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,2,2 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 32221-83:
(7*3)+(6*2)+(5*2)+(4*2)+(3*1)+(2*8)+(1*3)=73
73 % 10 = 3
So 32221-83-3 is a valid CAS Registry Number.

32221-83-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl (2S)-2-formamidopropanoate

1.2 Other means of identification

Product number -
Other names Alanine,N-formyl-,methyl ester (6CI,7CI)

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:32221-83-3 SDS

32221-83-3Relevant articles and documents

Capsicum annuum fruit extract: A novel reducing agent for the green synthesis of zno nanoparticles and their multifunctional applications

Lalithamba, Haraluru Shankraiah,Raghavendra, Mahadevaiah,Uma, Kogali,Yatish, Kalanakoppal Venkatesh,Mousumi, Das,Nagendra, Govindappa

, p. 354 - 364 (2018/07/05)

A simple, efficient and convenient method for the preparation of zinc oxide (ZnO) nanoparticle was described. Several parameters like size and morphology of the prepared nanoparticles were characterized thorough a variety of analytical techniques such as

Formamide Synthesis through Borinic Acid Catalysed Transamidation under Mild Conditions

Mohy El Dine, Tharwat,Evans, David,Rouden, Jacques,Blanchet, Jér?me

supporting information, p. 5894 - 5898 (2016/04/26)

A highly efficient and mild transamidation of amides with amines co-catalysed by borinic acid and acetic acid has been reported. A wide range of functionalised formamides was synthesized in excellent yields, including important chiral α-amino acid derivatives, with minor racemisation being observed. Experiments suggested that the reaction rely on a cooperative catalysis involving an enhanced boron-derived Lewis acidity rather than an improved Br?nsted acidity of acetic acid. Amide bonds are reputedly difficult to activate due to their high resonance stabilization. An unusual mild activation of dimethylformamide and formamide by borinic acid 1 (see scheme), illustrated by a general formylation of a wide range of amines, including chiral α-amino esters, has been reported.

ENOPEPTINS, USES THEREOF, AND METHODS OF SYNTHESIS THERETO

-

Page/Page column 76, (2012/10/18)

Provided herein are inventive enopeptin compounds of Formula (I): and pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof. Further provided are methods of preparation, use, and treatment.

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