108392-76-3

Basic information

• Product Name: D-4-CHLOROPHENYLGLYCINE HCL
• Synonyms: D-4-CHLOROPHENYLGLYCINE HCL;D-4-Chlorophenylglycine hydrochloride;(R)-2-aMino-2-(4-chlorophenyl)acetic acid hydrochloride;(2R)-2-amino-2-(4-chlorophenyl)acetic acid,hydrochloride;R-4-Chlorophenylglycine hydrochloride
• CAS NO: 108392-76-3
• Molecular Formula: C₈H₈ClNO₂*ClH
• Molecular Weight: 222.07
• Mol File: 108392-76-3.mol

Chemical Properties

• Melting Point: 240 °C (decomp)(Solv: ethyl acetate (141-78-6))
• Boiling Point: 357°Cat760mmHg
• Flash Point: 169.7°C
• Appearance: /
• Density: g/cm³
• Vapor Pressure: 1.02E-05mmHg at 25°C
• CAS DataBase Reference: D-4-CHLOROPHENYLGLYCINE HCL(CAS DataBase Reference)
• NIST Chemistry Reference: D-4-CHLOROPHENYLGLYCINE HCL(108392-76-3)
• EPA Substance Registry System: D-4-CHLOROPHENYLGLYCINE HCL(108392-76-3)

Safety Data

• Hazardous Substances Data: 108392-76-3(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
D-4-Chlorophenylglycine HCl is used as an intermediate in the synthesis of pharmaceutical compounds. Its unique chemical structure allows it to be incorporated into various drug molecules, contributing to their therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, D-4-Chlorophenylglycine HCl serves as an intermediate in the production of agrochemicals. Its presence in these compounds can enhance their effectiveness in protecting crops from pests and diseases.
Used in Dye and Pigment Industry:
D-4-Chlorophenylglycine HCl is utilized in the manufacturing of dyes and pigments due to its ability to impart color. Its chemical properties make it suitable for creating a variety of shades and hues in different applications.
Used in Polymer and Resin Production:
D-4-CHLOROPHENYLGLYCINE HCL is also employed in the production of polymers and resins, where it contributes to the formation of polymer chains and the overall properties of the final product. Its versatility in solubility allows it to be integrated into various polymer systems, enhancing their performance and functionality.

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

Upstream product

• 104-88-1 4-chlorobenzaldehyde 
• 121784-63-2 4-chloro-N-(2,3,4,6-tetra-O-pivaloyl-β-D-galactopyranosyl)benzylideneamine 
• 108365-46-4 4-chloro-N-(2,3,4,6-tetra-O-pivaloyl-β-D-galactopyranosyl)-D-phenylglycinotrile 

Relevant 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

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