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Cyclopentylpropionyl chloride
[CAS# 104-97-2]

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Identification
Classification Organic raw materials >> Carboxylic compounds and derivatives >> Carboxylic acid halide
Name Cyclopentylpropionyl chloride
Synonyms 3-Cyclopentylpropionyl chloride
Molecular Structure CAS # 104-97-2, Cyclopentylpropionyl chloride, 3-Cyclopentylpropionyl chloride
Molecular Formula C8H13ClO
Molecular Weight 160.64
CAS Registry Number 104-97-2
EC Number 203-257-9
SMILES C1CCC(C1)CCC(=O)Cl
Properties
Density 1.049
Boiling point 199-200 ºC
Refractive index 1.464
Flash point 194 ºF
Safety Data
Hazard Symbols symbol   GHS05 Danger    Details
Hazard Statements H314-H318    Details
Precautionary Statements P260-P264-P264+P265-P280-P301+P330+P331-P302+P361+P354-P304+P340-P305+P354+P338-P316-P317-P321-P363-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Skin corrosionSkin Corr.1BH314
Serious eye damageEye Dam.1H318
Specific target organ toxicity - single exposureSTOT SE3H335
Substances or mixtures corrosive to metalsMet. Corr.1H290
Transport Information UN 3265
SDS Available
up Discovory and Applicatios
Cyclopentylpropionyl chloride, a chlorinated organic compound with the molecular formula C8H13ClO, is a derivative of propionic acid where the propionyl group is bonded to a cyclopentane ring. This compound likely emerged during the mid-20th century as part of ongoing research into acyl chlorides and their applications in organic synthesis. The synthesis of cyclopentylpropionyl chloride involves the chlorination of cyclopentylpropionic acid using reagents such as thionyl chloride (SOCl2) or oxalyl chloride ((COCl)2). Its discovery provided chemists with a new reagent for introducing the cyclopentylpropionyl group into various molecular frameworks.

Cyclopentylpropionyl chloride is a valuable intermediate in the pharmaceutical industry. Its ability to introduce the cyclopentylpropionyl group into target molecules makes it useful in the synthesis of active pharmaceutical ingredients (APIs). This reactivity is particularly important in the development of drugs where specific acyl groups can significantly impact biological activity and pharmacokinetic properties. For instance, it is used in creating compounds with enhanced lipophilicity, improving their ability to cross cell membranes and increasing their efficacy.

In the agrochemical sector, cyclopentylpropionyl chloride is employed to synthesize herbicides, insecticides, and fungicides. The introduction of the cyclopentylpropionyl group can enhance the stability and effectiveness of these compounds. This modification helps in developing agrochemicals that are more potent against pests and diseases, thereby supporting higher agricultural yields and better crop protection.

Cyclopentylpropionyl chloride is used in the development of specialized polymers and advanced materials. By acylating various monomers, it helps create polymers with unique properties such as improved thermal stability, resistance to chemicals, and enhanced mechanical strength. These polymers are used in high-performance materials for coatings, adhesives, and composite materials.

In organic synthesis, cyclopentylpropionyl chloride serves as a versatile reagent for introducing acyl groups into molecules. It participates in Friedel-Crafts acylation reactions, forming ketones that are key intermediates in the synthesis of various organic compounds.

Cyclopentylpropionyl chloride is used in research and development to study acylation reactions and explore new chemical transformations. Its well-defined reactivity provides a reliable model for investigating reaction mechanisms and optimizing conditions for acylation processes.
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