Chemical Property of 5-Chlorovaleryl chloride
Chemical Property:
- Appearance/Colour:clear colourless to slightly yellow liquid
- Vapor Pressure:0.586mmHg at 25°C
- Refractive Index:n20/D 1.464(lit.)
- Boiling Point:188.9 °C at 760 mmHg
- Flash Point:76.3 °C
- PSA：17.07000
- Density:1.183 g/cm3
- LogP:2.16090
- Storage Temp.:Store below +30°C.
- Sensitive.:Moisture Sensitive
- Water Solubility.:reacts
- XLogP3:2
- Hydrogen Bond Donor Count:0
- Hydrogen Bond Acceptor Count:1
- Rotatable Bond Count:4
- Exact Mass:153.9952203
- Heavy Atom Count:8
- Complexity:72.8
- Purity/Quality:
-
99% *data from raw suppliers
5-Chlorovaleryl Chloride *data from reagent suppliers
Safty Information:
- Pictogram(s):
C,
T
- Hazard Codes:C,T
- Statements:
22-34-23-23/34
- Safety Statements:
26-36/37/39-45
- MSDS Files:
-
SDS file from LookChem
Total 1 MSDS from other Authors
Useful:
- Canonical SMILES:C(CCCl)CC(=O)Cl
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Description
5-Chlorovaleryl chloride is an important synthetic intermediate of pyrazole herbicides. 5-Chloropentanoyl chloride is used as the raw material of 1,1,7-trichloro-1-hepten-3-one, and then the third-generation pyrazole herbicides can be synthesized. Pyrazole herbicides have the characteristics of ultra-efficient herbicidal activity, high selectivity, extremely low mammalian toxicity and good environmental characteristics, and have become a hot spot in the research and development of herbicides in the world in recent years.
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Uses
5-Chlorovaleroyl chloride (5-CVC) has been used in the development and validation of a GC-FID method for the analysis of low level impurities present in 5-CVC. It has been used in the synthesis of anion-exchange resins by acylation of polystyrene/divinylbenzene and subsequent amination with trimethylamine. It is commonly used as alkylating agent in the synthesis of pharmaceutical intermediates and other specialty chemicals. 5-Chlorovaleroyl chloride (5-CVC) has been used in the development and validation of a GC-FID method for the analysis of low level impurities present in 5-CVC. It has been used in the synthesis of anion-exchange resins by acylation of polystyrene/divinylbenzene and subsequent amination with trimethylamine.
