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Benzyl chloroformate
[CAS# 501-53-1]

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Complete supplier list of Benzyl chloroformate
Identification
Classification Biochemical >> Amino acids and their derivatives >> Other protected amino acids
Name Benzyl chloroformate
Synonyms Carbobenzoxy chloride; Carbonochloride acid benzylester
Molecular Structure CAS # 501-53-1, Benzyl chloroformate, Carbobenzoxy chloride, Carbonochloride acid benzylester
Molecular Formula C8H7ClO2
Molecular Weight 170.59
CAS Registry Number 501-53-1
EC Number 207-925-0
SMILES C1=CC=C(C=C1)COC(=O)Cl
Properties
Density 1.195
Melting point -18 ºC
Refractive index 1.519
Boiling point 103 ºC (20 mm Hg)
Flash point 92 ºC
Water solubility decomposes
Safety Data
Hazard Symbols symbol symbol symbol   GHS05;GHS06;GHS09 Danger    Details
Hazard Statements H314-H318-H330-H400-H410    Details
Precautionary Statements P260-P264-P264+P265-P271-P273-P280-P284-P301+P330+P331-P302+P361+P354-P304+P340-P305+P354+P338-P316-P317-P320-P321-P363-P391-P403+P233-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Acute hazardous to the aquatic environmentAquatic Acute1H400
Chronic hazardous to the aquatic environmentAquatic Chronic1H410
Skin corrosionSkin Corr.1BH314
Serious eye damageEye Dam.1H318
Acute toxicityAcute Tox.2H330
Specific target organ toxicity - single exposureSTOT SE3H335
CarcinogenicityCarc.1BH350
CarcinogenicityCarc.1AH350
Transport Information UN 1739
SDS Available
up Discovory and Applicatios
Benzyl chloroformate, with the chemical formula C8H7ClO2, is an organofluorine compound commonly used as a reagent in organic synthesis. It consists of a benzyl group attached to a chloroformate moiety, making it a valuable tool in various chemical transformations. The discovery and development of benzyl chloroformate have significantly impacted its applications in organic chemistry, including its use in the synthesis of esters, carbonates, and other functional groups.

The discovery of benzyl chloroformate can be traced back to advancements in the chemistry of chloroformates and their derivatives. Chloroformates, known for their reactivity with alcohols and amines, have been used extensively as intermediates in organic synthesis. The introduction of the benzyl group into chloroformates provided a compound with enhanced reactivity and selectivity. The synthesis of benzyl chloroformate typically involves the reaction of benzyl alcohol with phosgene, resulting in the formation of the chloroformate ester.

In organic synthesis, benzyl chloroformate serves as a versatile reagent. One of its primary applications is in the protection of alcohols and amines during multi-step syntheses. By reacting with alcohols, benzyl chloroformate forms benzyl esters, which are stable and can be easily removed after the desired transformations are completed. Similarly, it can react with amines to form benzyl carbamates, which are used to protect amino groups during complex syntheses. This protective strategy is crucial for ensuring selective reactions and preventing undesired side reactions.

Benzyl chloroformate also plays a role in the synthesis of various pharmaceuticals and fine chemicals. Its ability to introduce carbonyl groups into molecules makes it valuable in the preparation of carbonates and carbamates, which are important functional groups in drug development. Additionally, it is used in the synthesis of polymer precursors and other specialty chemicals, further demonstrating its utility in the chemical industry.

In summary, benzyl chloroformate is a significant reagent in organic chemistry, offering valuable applications in the protection of functional groups and the synthesis of complex molecules. Its discovery and development have enhanced the capabilities of organic synthesis, making it an essential tool in the preparation of pharmaceuticals, polymers, and other fine chemicals.
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