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Catalog Number:
26762
CAS Number:
4252-78-2
2,4-Dichloro-α-chloroacétophénone
Purity:
≥ 99% (GC)
Synonym(s):
Chlorure de 2,4-dichlorophénacyle, 2,2',4'-Trichloroacétophénone
Hazmat
Documents
$20.00 /25G
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Product Information

Utilisation comme pesticide et intermédiaire médical, dans la préparation du nitrate de miconazole et du nitrate d'éconazole par thionation de composés carbonylés.

Synonyms
Chlorure de 2,4-dichlorophénacyle, 2,2',4'-Trichloroacétophénone
CAS Number
4252-78-2
Purity
≥ 99% (GC)
Molecular Formula
C8H5Cl3O
Molecular Weight
223.49
MDL Number
MFCD00000934
PubChem ID
20250
Melting Point
47-54 ?C
Appearance
Cristal blanc à blanc pâle
Boiling Point
130-135 ?C
Conditions
Conserver à 0-8 °C
Warnings
Danger.
General Information
Synonyms
Chlorure de 2,4-dichlorophénacyle, 2,2',4'-Trichloroacétophénone
CAS Number
4252-78-2
Purity
≥ 99% (GC)
Molecular Formula
C8H5Cl3O
Molecular Weight
223.49
MDL Number
MFCD00000934
PubChem ID
20250
Melting Point
47-54 ?C
Appearance
Cristal blanc à blanc pâle
Boiling Point
130-135 ?C
Conditions
Conserver à 0-8 °C
Warnings
Danger.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Oui
Antibiotic
Non
DEA-regulated
Non
Warnings
Danger.
Applications

2,4-Dichloro-a-chloroacetophenone is widely utilized in research focused on:

  • Pesticide Development: This compound serves as a key intermediate in the synthesis of various pesticides, helping to enhance agricultural productivity by effectively controlling pests.
  • Pharmaceutical Research: It is used in the development of pharmaceutical agents, particularly in creating compounds with anti-inflammatory and analgesic properties, benefiting the healthcare industry.
  • Chemical Synthesis: The compound acts as a versatile building block in organic synthesis, allowing chemists to create more complex molecules efficiently, which is crucial in materials science and polymer development.
  • Laboratory Reagents: It functions as a reagent in various chemical reactions, providing researchers with reliable tools for studying reaction mechanisms and developing new chemical processes.
  • Environmental Studies: This chemical is utilized in environmental research to assess the degradation of chlorinated compounds, aiding in the understanding of their impact on ecosystems and informing remediation strategies.

Citations