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Structure

Isopropyl(4-Chlorophenyl)Acetyl Chloride

CAS
51631-50-6
Catalog Number
ACM51631506
Category
Other Products
Molecular Weight
231.12
Molecular Formula
C11H12Cl2O

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Specification

Synonyms
Isopropyl(4-chlorophenyl)acetyl chloride, 51631-50-6, 2-(4-Chlorophenyl)-3-methylbutyryl chloride, 3-Methyl-2-(4-chlorophenyl)butyryl chloride, 2-(4-chlorophenyl)-3-methylbutanoyl chloride, ACMC-20aopk, AC1N4FF9, AGN-PC-00DFQ6, KSC496K9B, 537225_ALDRICH, CTK3J6590, AKOS015890780, AG-F-74996, P804, KB-183508, FT-0640010, A23956, (2S)-2-(4-chlorophenyl)-3-methylbutanoyl chloride, I01-7769, (4-Chlorophenyl)-a-isopropylacetyl chloride;2-(4-Chlorophenyl)-3-methylbutanoyl chloride; 2-(4-Chlorophenyl)-3-methylbutyrylchloride; 2-(4-Chlorophenyl)isovaleryl chloride;2-(p-Chlorophenyl)-3-methylbutyryl chloride; 2-(p-Chlorophenyl)isovaleroylchloride; 3-Methyl-2-(4-chlorophenyl)butanoyl chloride;Isopropyl(4-chlorophenyl)acetyl chloride; a-Isopropyl-4-chlorophenylacetyl chloride
IUPAC Name
2-(4-chlorophenyl)-3-methylbutanoyl chloride
Canonical SMILES
CC(C)C(C1=CC=C(C=C1)Cl)C(=O)Cl
InChI Key
BWPYAVCZZUTOBY-UHFFFAOYSA-N
Boiling Point
124-130ºC (3 Torr)
Flash Point
117ºC
Density
1.195
Exact Mass
230.02700
Hazard Statements
Xi
H-Bond Acceptor
1
H-Bond Donor
0
Safety Description
S26
WGK Germany
3

Downstream Synthesis Route 1

  • 51631-50-6
  • 2012-74-0

Reference: [1] Patent: US4228172, 1980, A,

Downstream Synthesis Route 2

  • 51176-48-8
  • 51631-50-6
  • 51629-80-2

Reference: [1]Patent: FR2216919,1974,B1

Downstream Synthesis Route 3

  • 35714-19-3
  • 51631-50-6
  • 51630-57-0

Reference: [1]Patent: FR2216919,1974,B1

Downstream Synthesis Route 4

  • 4494-85-3
  • 51631-50-6
  • 51629-78-8

Reference: [1]Patent: FR2216919,1974,B1

* For details of the synthesis route, please refer to the original source to ensure accuracy.

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