65448-20-6

Basic information

• Product Name: 4-(2-chloro-2-oxoethyl)phenyl acetate
• CAS NO: 65448-20-6
• Molecular Formula: C₁₀H₉ClO₃
• Molecular Weight: 212.6297
• Mol File: 65448-20-6.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 307.6°C at 760 mmHg
• Flash Point: 130.5°C
• Density: 1.262g/cm³
• Vapor Pressure: 0.000717mmHg at 25°C
• Refractive Index: 1.53
• CAS DataBase Reference: 4-(2-chloro-2-oxoethyl)phenyl acetate(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(2-chloro-2-oxoethyl)phenyl acetate(65448-20-6)
• EPA Substance Registry System: 4-(2-chloro-2-oxoethyl)phenyl acetate(65448-20-6)

Safety Data

• Hazardous Substances Data: 65448-20-6(Hazardous Substances Data)

Upstream product

• 38177-33-2 (4-acetoxyphenyl)acetic acid 
• 156-38-7 4-hydroxyphenylacetate 
• 1197-55-3 4-aminophenylacetic acid 
• 79145-99-6 3-(4-hydroxy-phenyl)-2-thioxo-propionic acid 
• 56401-28-6 [2-hydroxyimino-3-(4-hydroxyphenyl)]propionic acid 
• 67741-16-6 O-acetyl-4-hydroxyphenylacetonitrile 
• 79-37-8 oxalyl dichloride 

Downstream Products

• 858819-14-4 (4-acetoxy-phenyl)-acetic acid-(2,2-diethoxy-ethylamide) 
• 87783-78-6 2-(2-phenylvinyl)-4-benzyl-5-((p-acetoxyphenyl)acetamido)oxazole 
• 131691-05-9 (4-Acetoxy-phenyl)-acetic acid 2-(2-methyl-5-nitro-imidazol-1-yl)-ethyl ester 
• 149110-60-1 1,4,-benzodioxan-2-ylmethyl 4-acetoxyphenylacetate 
• 52727-20-5 4-(3-Diazo-2-oxo-propyl)phenyl acetate 
• 29515-28-4 1-Hydroxy-3-(4-hydroxyphenyl)-propan-2-one 
• 360077-62-9 4-(4-Acetoxy-phenyl)-2-oxo-propyl trifluoroacetate 
• 56071-70-6 3-(p-acetoxyphenyl)-2-oxopropanal 
• 56071-69-3 acetic acid 4-(3-bromo-2-oxo-propyl)phenyl ester 
• 187961-94-0 acetic acid 4-(3-nitrooxy-2-oxo-propyl)phenyl ester 
• 55779-48-1 coelenterazine 
• 149110-55-4 1,4,-benzodioxan-2-ylmethyl 4-hydroxyphenylacetate 

Relevant articles and documents

Preparation of α-amino acids by oxidative oxazoline-oxazinone rearrangement-hydrogenation (OOOH). Scope and limitations

The range and scope of the oxidative oxazoline-oxazinone rearrangement-hydrogenation sequence (OOOH)-a short, direct asymmetric synthesis of α-amino acids from carboxylic acids-was explored. The highest yet reported diastereoselectivity for hydrogenation of the oxazinone C=N bond (d.r.=>80:1) is disclosed and rationalized with the aid of ab initio molecular calculations.

New cyclohexadienone derivatives: Preparation and chiral discrimination in high-pressure diels - Alder cycloadditions

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