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Benzeneacetamide, N-(2-amino-1-methyl-2-oxoethyl)-, (S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65451-29-8

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65451-29-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65451-29-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,4,5 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 65451-29:
(7*6)+(6*5)+(5*4)+(4*5)+(3*1)+(2*2)+(1*9)=128
128 % 10 = 8
So 65451-29-8 is a valid CAS Registry Number.

65451-29-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-2-(2-phenylacetamido)propanamide

1.2 Other means of identification

Product number -
Other names Phac-Ala-NH2

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:65451-29-8 SDS

65451-29-8Downstream Products

65451-29-8Relevant academic research and scientific papers

GRANZYME B DIRECTED IMAGING AND THERAPY

-

Page/Page column 82; 97, (2019/09/04)

Provided herein are heterocyclic compounds useful for imaging Granzyme B. Methods of imaging Granzyme B, combination therapies, and kits comprising the Granzyme B imaging agents are also provided.

B(OCH2CF3)3-mediated direct amidation of pharmaceutically relevant building blocks in cyclopentyl methyl ether

Karaluka, Valerija,Lanigan, Rachel M.,Murray, Paul M.,Badland, Matthew,Sheppard, Tom D.

supporting information, p. 10888 - 10894 (2015/11/17)

The use of B(OCH2CF3)3 for mediating direct amidation reactions of a wide range of pharmaceutically relevant carboxylic acids and amines is described, including numerous heterocycle-containing examples. An initial screen of solvents for the direct amidation reaction suggested that cyclopentyl methyl ether, a solvent with a very good safety profile suitable for use over a wide temperature range, was an excellent replacement for the previously used solvent acetonitrile. Under these conditions amides could be prepared from 18 of the 21 carboxylic acids and 18 of the 21 amines examined. Further optimisation of one of the low yielding amidation reactions (36% yield) via a design of experiments approach enabled an 84% yield of the amide to be obtained.

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