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2-Phenylbutyryl chloride

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2-Phenylbutyryl chloride Basic information

Product Name:
2-Phenylbutyryl chloride
Synonyms:
  • 2-PHENYLBUTYRYL CHLORIDE
  • 2-PHENYLBUTYRIC CHLORIDE
  • 2-ETHYL-2-PHENYLACETYL CHLORIDE
  • 2-phenylbutyril chloride
  • INTERMEDIATES FORBUTAMITRATE,FENBATRAZATE,PHENETURIDE
  • 2-Phenyl Butyric acid Chloride
  • 2-Phenylbutyryl hloride
  • 2PhenylButylrylChloride
CAS:
36854-57-6
MF:
C10H11ClO
MW:
182.65
EINECS:
253-241-0
Product Categories:
  • Miscellaneous
  • Acid Halides
  • Carbonyl Compounds
  • Organic Building Blocks
  • Acid Halides
  • Building Blocks
  • Carbonyl Compounds
  • Chemical Synthesis
  • Organic Building Blocks
Mol File:
36854-57-6.mol
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2-Phenylbutyryl chloride Chemical Properties

Melting point:
178-180 °C
Boiling point:
122-125 °C/20 mmHg (lit.)
Density 
1.093 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.516(lit.)
Flash point:
209 °F
storage temp. 
Inert atmosphere,Room Temperature
solubility 
Chloroform, Hexanes
form 
Oil
color 
Colourless to Light Yellow
Specific Gravity
1.090
Sensitive 
Moisture Sensitive
BRN 
2045209
CAS DataBase Reference
36854-57-6(CAS DataBase Reference)
NIST Chemistry Reference
2-Phenylbutyryl chloride(36854-57-6)
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Safety Information

Hazard Codes 
C
Risk Statements 
34
Safety Statements 
22-26-27-36/37/39-45
RIDADR 
UN 3265 8/PG 2
WGK Germany 
3
RTECS 
ET5957500
HazardClass 
8
PackingGroup 
II
HS Code 
29130000

MSDS

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2-Phenylbutyryl chloride Usage And Synthesis

Chemical Properties

Clear pale yellow to yellow liquid

Uses

α-Ethyl-benzeneacetyl Chloride is used in the synthesis of mild and neutral system for selective reduction of organic functional groups. Also used in the preparation of phenothiazine derivatives for the reversible inhibition of human butyrylcholinesterase.

Uses

(R)-(-)-2-phenylbutyryl chloride may be employed as chiral reagent for the determination of dopamine and dopamine-derived salsolinol and norsalsolinol in human brain by GC-MS method. Chiral (S)-(+)-2-phenylbutyryl chloride may be used as derivatization reagent for the hydroxyl groups during the GC-MS assay for the enantiomers of 1,2-propanediol, 1,3-butanediol, 1,3-pentanediol and their corresponding hydroxyacids in biological fluids.

General Description

The kinetic resolution of racemic 2-phenylbutyryl chloride by sterically hindered chiral secondary alcohols has been evaluated. 2-Phenylbutyryl chloride reacts with 4-methoxybenzoyl chloride catalyzed by PdBr(Ph)(PPh3)2 to yield 1-(4-methoxyphenyl)-2-phenyl-2-buten-1-one.

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