Skip to content
chloroformate
EntityQ2746231· pop 12· linked from 20 articles

chloroformate

Sign in to save

Also known as chloroformates

thumb|right|General chemical structure of chloroformate esters Chloroformates are a class of organic compounds with the formula ROC(O)Cl. They are formally esters of chloroformic acid. Most are colorless, volatile liquids that degrade in moist air. A simple example is methyl chloroformate, which is commercially available.

Wikidata facts

Show 2 more facts
Commons category
Chloroformate esters
topic's main category
Category:Chloroformates
Sources (3)

via Wikidata · CC0

~2 min read

Encyclopedic overview

2 sections
Contents
  • Reactions
  • References

thumb|right|General chemical structure of chloroformate esters Chloroformates are a class of organic compounds with the formula ROC(O)Cl. They are formally esters of chloroformic acid. Most are colorless, volatile liquids that degrade in moist air. A simple example is methyl chloroformate, which is commercially available.

Chloroformates are used as reagents in organic chemistry. For example, benzyl chloroformate is used to introduce the Cbz (carboxybenzyl) protecting group and fluorenylmethyloxycarbonyl chloride is used to introduce the FMOC protecting group. Chloroformates are popular in the field of chromatography as derivatization agents. They convert polar compounds into less polar more volatile derivatives. In this way, chloroformates enable relatively simple transformation of large array of metabolites (aminoacids, amines, carboxylic acids, phenols) for analysis by gas chromatography / mass spectrometry.

Excerpted from Wikipedia’s “chloroformate” article, available under the CC BY-SA 4.0 licence.