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Propyl chloroformate
[CAS# 109-61-5]

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Complete supplier list of Propyl chloroformate
Identification
Classification Chemical reagent >> Organic reagent >> Ester >> Propyl esters
Name Propyl chloroformate
Synonyms n-Propyl Chloroformate; Carbonochloridic acid propyl ester; Chloroformic acid propyl ester
Molecular Structure CAS # 109-61-5, Propyl chloroformate, n-Propyl Chloroformate, Carbonochloridic acid propyl ester, Chloroformic acid propyl ester
Molecular Formula C4H7ClO2
Molecular Weight 122.55
CAS Registry Number 109-61-5
EC Number 203-687-7
SMILES CCCOC(=O)Cl
Properties
Density 1.09
Boiling point 105-106 ºC
Refractive index 1.404
Flash point 84 ºF
Safety Data
Hazard Symbols symbol symbol symbol   GHS02;GHS06;GHS05 Danger    Details
Hazard Statements H225-H331-H314    Details
Precautionary Statements P210-P233-P240-P241-P242-P243-P260-P261-P264-P264+P265-P270-P271-P280-P284-P301+P317-P301+P330+P331-P302+P361+P354-P303+P361+P353-P304+P340-P305+P354+P338-P316-P317-P320-P321-P330-P363-P370+P378-P403+P233-P403+P235-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Skin corrosionSkin Corr.1BH314
Flammable liquidsFlam. Liq.2H225
Acute toxicityAcute Tox.4H302
Serious eye damageEye Dam.1H318
Acute toxicityAcute Tox.2H330
Acute toxicityAcute Tox.3H331
Transport Information UN 2740
SDS Available
up Discovory and Applicatios
Propyl chloroformate is an organic compound with the chemical formula C4H7ClO2. It is a colorless liquid that is primarily used as a reagent in organic synthesis. The chloroformate group, combined with a propyl chain, makes it highly reactive and useful in the formation of esters and carbamates. Propyl chloroformate is a valuable intermediate in producing various chemical compounds, particularly in pharmaceuticals and agrochemicals.

The discovery of propyl chloroformate is rooted in the exploration of chloroformates, a class of compounds known for their ability to introduce ester and carbamate functionalities. This reactivity makes them vital in modifying molecules, especially in drug development and peptide synthesis. Propyl chloroformate is specifically known for its use in coupling reactions, where it reacts with alcohols to form esters and with amines to form carbamates.

In peptide synthesis, propyl chloroformate is utilized as a coupling reagent to protect or modify amino acids during the formation of peptide bonds. Its ability to react selectively with functional groups in amino acids ensures smooth peptide elongation without unwanted side reactions. The compound's reactivity and versatility in protecting groups during peptide assembly have made it a standard tool in biochemical research.

In the pharmaceutical industry, propyl chloroformate is applied in the synthesis of drug intermediates. Its use allows for the efficient formation of key intermediates in active pharmaceutical ingredients, where control over chemical reactivity is crucial. The introduction of ester or carbamate functionalities through propyl chloroformate often improves the stability or bioavailability of drug molecules.

Propyl chloroformate is also employed in the agrochemical industry. It participates in the synthesis of carbamate-based pesticides, which are known for their effectiveness in pest control. The ability of propyl chloroformate to form stable carbamates ensures the long-term stability and efficacy of these products in agricultural settings.

Overall, propyl chloroformate continues to be a widely used reagent due to its reactivity, especially in esterification and carbamate formation. Its role in the synthesis of complex molecules highlights its importance in both research and industry.
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