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49782-76-5

3-chlorophenyl chloroformate

Catalog#: AR01B43F  |   CAS#: 49782-76-5  |   MDL#: MFCD24141155  |   MF: C7H4Cl2O2  |   MW: 191.0115

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Catalog Number AR01B43F
Chemical Name 3-chlorophenyl chloroformate
CAS Number 49782-76-5
Molecular Formula C7H4Cl2O2
Molecular Weight 191.0115
MDL Number MFCD24141155
SMILES ClC(=O)Oc1cccc(c1)Cl

3-Chlorophenyl carbonochloridate, also known as 3-chlorophenyl chloroformate, is a versatile chemical compound widely used in chemical synthesis for various applications. This compound serves as a key building block in organic synthesis due to its unique reactivity and functional groups. One important application of 3-Chlorophenyl carbonochloridate is its utilization as a acyl chloride in the formation of amides. By reacting with amines, this compound can undergo acylation reactions to form amide bonds, which are crucial in peptide synthesis and pharmaceutical research. The high reactivity of the carbonochloridate group allows for efficient and selective amide bond formation under mild conditions.Additionally, 3-Chlorophenyl carbonochloridate can be employed in the preparation of esters through esterification reactions with alcohols. The chloroformate group readily reacts with alcohol groups to form ester linkages, which are essential in the production of various organic compounds including fragrances, flavorings, and pharmaceuticals.Furthermore, this compound can be used as a protecting group in organic synthesis to selectively mask hydroxyl or amino functional groups. The chloroformate moiety can be easily removed under mild conditions, allowing for the precise manipulation of functional groups during multi-step synthesis processes.Overall, the versatile reactivity and functionality of 3-Chlorophenyl carbonochloridate make it a valuable tool in chemical synthesis, enabling the efficient production of a wide range of organic compounds with diverse applications.
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