H-PHG(4-CL)-OH

H-PHG(4-CL)-OH - Names and Identifiers

Name	(2S)-amino(4-chlorophenyl)ethanoic acid
Synonyms	L-4-Cl-Phg-OH H-Phg(4-Cl)-OH H-PHG(4-CL)-OH (4-CHLOROPHENYL)GLYCINE L-4-CHLOROPHENYLGLYCINE PARACHLOROPHENYLGLYCINE (S)-4-CHLOROPHENYL GLYCINE (S)-2-(4-Chlorophenyl)glycine AMINO-(4-CHLORO-PHENYL)-ACETIC ACID (2S)-Amino(4-chlorophenyl)acetic acid (S)-Amino-(4-Chloro-Phenyl)-Acetic Acid (S)-AMINO-(4-CHLORO-PHENYL)-ACETIC ACID (2S)-amino(4-chlorophenyl)ethanoic acid Benzeneacetic acid, alpha-amino-4-chloro-, (alphaS)-
CAS	67336-19-0
InChI	InChI=1/C8H8ClNO2/c9-6-3-1-5(2-4-6)7(10)8(11)12/h1-4,7H,10H2,(H,11,12)/t7-/m0/s1

H-PHG(4-CL)-OH - Physico-chemical Properties

Molecular Formula	C8H8ClNO2
Molar Mass	185.61
Density	1.392±0.06 g/cm3(Predicted)
Melting Point	229 °C
Boling Point	328.8±32.0 °C(Predicted)
Flash Point	152.7°C
Vapor Presure	7.45E-05mmHg at 25°C
Appearance	powder to crystal
Color	White to Almost white
pKa	1.81±0.10(Predicted)
Storage Condition	Sealed in dry,Room Temperature
Refractive Index	1.603

H-PHG(4-CL)-OH - Risk and Safety

Hazard Symbols	T - Toxic
Risk Codes	25 - Toxic if swallowed
Safety Description	45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)

H-PHG(4-CL)-OH - Introduction

(2S)-amino (4-Chlorophenyl) ethanoic acid is an organic compound with the chemical formula (C2H5)2NCH(COOH)(C6H4Cl). The following is a description of its nature, use, formulation and safety information:

Nature:
(2S)-amino(4-chlorophenyl)ethanoic acid is a white crystalline solid that does not volatilize at room temperature. Its melting point is about 200-220 degrees Celsius. It is an optically active compound with one chiral center and exists as two stereoisomers:(2S)-amino(4-chlorophenyl)ethanoic acid and (R)-4-chlorophenylglycine.

Use:
(2S)-amino(4-chlorophenyl)ethanoic acid is a chiral amino acid, widely used in medicine and organic synthesis. It can be used as a drug intermediate, chiral catalyst and ligand, which is helpful for the synthesis of chemicals and the preparation of drugs.

Preparation Method:
(2S)-amino(4-chlorophenyl)ethanoic acid can be synthesized by the carbene leaf condensation reaction of benzaldehyde and phenethylamine. The experimental conditions can be adjusted according to the specific synthesis requirements.

Safety Information:
(2S)-amino (4-Chlorophenyl) ethanoic acid is a relatively safe compound under general operating conditions. However, as an organic compound, the following should be noted when using and handling:
-Avoid contact with skin, eyes and respiratory tract. Wear appropriate personal protective equipment such as laboratory gloves, safety glasses and protective masks when handling.
-Follow good laboratory safety procedures during operation, ensure good ventilation, and avoid fire sources and static electricity accumulation.
-Store dry, sealed and away from fire and oxidizing agents.
-Before use, handling and disposal, the relevant safety data sheets and operating instructions should be read and observed.

Please note that the above information only provides basic reference, and specific safety operations should be evaluated and planned according to experimental conditions and usage occasions.

Last Update：2024-04-09 20:45:29