35373-63-8

Basic information

• Product Name: DL-4-CHLOROPHENYLALANINOL
• Synonyms: DL-4-CHLOROPHENYLALANINOL;2-AMINO-3-(4-CHLOROPHENYL)-1-PROPANOL;TIMTEC-BB SBB000254;(±)-2-amino-3-(p-chlorophenyl)propanol;(±)-2-(p-chlorophenyl)-1-[hydroxymethyl)ethylamine;2-Amino-3-(4-chlorophenyl)-1-propanol, (±)-2-(p-Chlorophenyl)-1-[hydroxymethyl)ethylamine;(±)-β-Amino-4-chlorobenzene-1-propanol;rac-(R*)-3-(4-Chlorophenyl)-2-amino-1-propanol
• CAS NO: 35373-63-8
• Molecular Formula: C₉H₁₂ClNO
• Molecular Weight: 185.65
• EINECS: 252-533-5
• Product Categories: Amino Alcohols;Building Blocks;Chemical Synthesis;Organic Building Blocks;Oxygen Compounds
• Mol File: 35373-63-8.mol
• Article Data: 1

Chemical Properties

• Melting Point: 80-82 °C(lit.)
• Boiling Point: 338.4 °C at 760 mmHg
• Flash Point: 158.5 °C
• Appearance: /
• Density: 1.219±0.06 g/cm3 (20 ºC 760 Torr)
• Vapor Pressure: 3.82E-05mmHg at 25°C
• Refractive Index: 1.575
• Storage Temp.: 2-8°C
• CAS DataBase Reference: DL-4-CHLOROPHENYLALANINOL(CAS DataBase Reference)
• NIST Chemistry Reference: DL-4-CHLOROPHENYLALANINOL(35373-63-8)
• EPA Substance Registry System: DL-4-CHLOROPHENYLALANINOL(35373-63-8)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26
• WGK Germany: 3
• Hazardous Substances Data: 35373-63-8(Hazardous Substances Data)

Usage

Uses

DL-4-Chlorophenylalaninol may be used in chemical synthesis.

InChI:InChI=1/C9H12ClNO/c10-8-3-1-7(2-4-8)5-9(11)6-12/h1-4,9,12H,5-6,11H2/t9-/m0/s1

Upstream product

• 7424-00-2 DL-Phe(4Cl) 

Downstream Products

• 1072197-49-9 C₁₃H₁₄ClNO₃ 
• 913718-36-2 2-chloro-N-[1-(4-chlorobenzyl)-2-hydroxyethyl]acetamide 
• 913718-38-4 5-(4-chlorobenzyl)morpholine 
• 849106-44-1 4-(4-chloro-benzyl)-3-piperidin-4-yl-oxazolidin-2-one 
• 849106-43-0 4-[4-(4-chloro-benzyl)-2-oxo-oxazolidin-3-yl]-piperidine-1-carboxylic acid tert-butyl ester 
• 201864-00-8 (1S)-1-(4-chlorophenylmethyl)-2-hydroxyethylamine 
• 201863-99-2 (R)-2-amino-3-(4-chlorophenyl)propan-1-ol 

Relevant articles and documents

A catalyst-free, convenient construction of eight-membered [1,4]oxazocane-5,8-dione heterocycles from aminoethanols with divinyl succinate

A convenient protocol for the synthesis of [1,4]oxazocane-5,8-dione heterocycles by direct cyclization using 2-substituted aminoethanols and divinyl succinate without any catalysts and additives was established. This strategy is quite simple and effective to obtain eight-membered rings incorporating lactone and lactam functional groups. Georg Thieme Verlag Stuttgart.