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108392-76-3

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108392-76-3 Usage

General Description

D-4-Chlorophenylglycine HCl is a chemical compound that belongs to the class of organic compounds known as phenylglycines. It is a derivative of phenylglycine that contains a chlorine atom at the 4-position on the phenyl ring, and is found in the form of a hydrochloride salt. D-4-CHLOROPHENYLGLYCINE HCL has various industrial and pharmaceutical applications, including as an intermediate in the synthesis of pharmaceutical compounds and agrochemicals. It is also used in the manufacturing of dyes and pigments, as well as in the production of polymers and resins. D-4-Chlorophenylglycine HCl is a white to off-white crystalline powder that is soluble in water and organic solvents.

Check Digit Verification of cas no

The CAS Registry Mumber 108392-76-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,3,9 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 108392-76:
(8*1)+(7*0)+(6*8)+(5*3)+(4*9)+(3*2)+(2*7)+(1*6)=133
133 % 10 = 3
So 108392-76-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H8ClNO2.ClH/c9-6-3-1-5(2-4-6)7(10)8(11)12;/h1-4,7H,10H2,(H,11,12);1H/t7-;/m1./s1

108392-76-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R)-2-amino-2-(4-chlorophenyl)acetic acid,hydrochloride

1.2 Other means of identification

Product number -
Other names (R)-2-amino-2-(4-chlorophenyl)acetic acid hydrochloride

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:108392-76-3 SDS

108392-76-3Downstream Products

108392-76-3Relevant articles and documents

Carbohydrates as Chiral Templates: Stereoselective Strecker Synthesis of D-α-Amino Nitriles and Acids Using O-Pivaloylated D-Galactosylamine as the Auxiliary

Kunz, Horst,Sager, Wilfried,Schanzenbach, Dirk,Decker, Mathias

, p. 649 - 654 (2007/10/02)

The asymmetric synthesis of N-galactosyl D-α-amino nitriles is accomplished by application of 2,3,4,6-tetra-O-pivaloyl-β-D-galactopyranosylamine (4) as the stereodifferentiating template in Strecker reactions.Aldimines 6 derived from 4 and aromatic or ali

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