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N-(2-Chloroacetyl)-2-methylalanine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

95038-11-2

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95038-11-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95038-11-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,0,3 and 8 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 95038-11:
(7*9)+(6*5)+(5*0)+(4*3)+(3*8)+(2*1)+(1*1)=132
132 % 10 = 2
So 95038-11-2 is a valid CAS Registry Number.

95038-11-2SDS

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 2-[(2-chloroacetyl)amino]-2-methylpropanoic acid

1.2 Other means of identification

Product number -
Other names 2-(2-chloro acetylamino)-2-methyl Propionic Acid

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:95038-11-2 SDS

95038-11-2Relevant academic research and scientific papers

Ring-opened azlactone initiators for atom transfer radical polymerization

-

, (2008/06/13)

Initiators for atom transfer radical polymerizations are described. The initiators have an azlactone or ring-opened azlactone moiety to provide telechelic (co)polymers.

LINEAR OLIGOPEPTIDES. CXXII. FIRST SOLID-STATE STRUCTURAL ANALYSIS OF A COMPLETE Nα-MONO-, DI-, AND TRI-HALOACETYLATED α-AMINO ACID SERIES

Valle, Giovanni,Bonora, Gian Maria,Toniolo, Claudio

, p. 481 - 486 (2007/10/02)

A solid-state structural analysis of Nα-mono-, di-, and tri-chloroacetyl-α-aminoisobutyric acid derivatives was performed using X-ray diffraction.In all three structures the α-aminoisobutyryl residues shows a φ, ψT set of torsion angles falling in the region of the Ramachandran map where α- and 310-helices are found.The conformation of the amide bond (torsion angle ω) is always trans and the substituted acetamido and carboxylic acid groups are nearly perpendicular to each other.The conformation of the chloroacetamido group is always such that all chlorine atoms tend to reside far from the nitrogen atom.There are no intramolecular hydrogen bonds in the three structures.The intramolecular hydrogen bonding schemes for the three chloroacetylated derivatives are different.

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