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2-[Methyl(2-phenylacetyl)amino]acetic acid is a complex organic compound with the molecular formula C12H15NO3. It is a derivative of acetic acid, featuring a methyl group attached to the nitrogen atom of an amide group, which is in turn connected to a phenyl ring. 2-[Methyl(2-phenylacetyl)amino]acetic acid is known for its potential applications in pharmaceuticals and as a chemical intermediate. It is characterized by its ability to form salts and esters, which can be used in the synthesis of various drugs and other chemical products. The compound's structure and properties make it a versatile building block in organic chemistry, particularly in the development of new medications and other specialty chemicals.

155256-51-2

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155256-51-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 155256-51-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,2,5 and 6 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 155256-51:
(8*1)+(7*5)+(6*5)+(5*2)+(4*5)+(3*6)+(2*5)+(1*1)=132
132 % 10 = 2
So 155256-51-2 is a valid CAS Registry Number.

155256-51-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[Methyl(2-phenylacetyl)amino]acetic acid

1.2 Other means of identification

Product number -
Other names N-phenylacetyl-glycine nitrile

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:155256-51-2 SDS

155256-51-2Relevant academic research and scientific papers

Convenient synthesis of 4-trifluoromethyl-substituted imidazole derivatives

Kawase,Saito,Kurihara

, p. 461 - 464 (2007/10/03)

Mesoionic 4-trifluoroacetyl-1,3-oxazolium-5-olates (1), obtained from the reaction of N-acyl-N-alkylglycines (2) with trifluoroacetic anhydride, react with ammonia to give 4-trifluoromethyl-3,4-dihydroimidazoles (3) in high yields. Dehydration of 3 gives

Intermolecular 1,3-dipolar cycloadditions of muechnones with acetylenic dipolarophiles: Sorting out the regioselectivity

Coppola, Brian P.,Noe, Mark C.,Schwartz, David J.,Abdon II, Robert L.,Trost, Barry M.

, p. 93 - 116 (2007/10/02)

A series of 1,3-dipolar cycloadditions of muenchnones with acetylenic dipolarophiles was studied, wherein factors related to regioselectivity were investigated. The results from muenchnones with electronically divergent thioaryl substituents compared with

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