Chloroformylhexanoic acid ethyl ester, with the CAS number 14794-32-2, is an organic compound characterized by its ester functional group and the presence of a chloroformyl moiety. This compound typically appears as a colorless to pale yellow liquid and is known for its moderate volatility and solubility in organic solvents. It is often utilized in organic synthesis and as an intermediate in the production of various pharmaceuticals and agrochemicals. The presence of the chloroformyl group suggests reactivity, particularly in nucleophilic substitution reactions, making it a valuable building block in synthetic chemistry. Additionally, the ethyl ester component contributes to its relatively low boiling point compared to other carboxylic acid derivatives. Safety considerations are important when handling this compound, as it may pose health risks through inhalation or skin contact, necessitating appropriate protective measures. Overall, chloroformylhexanoic acid ethyl ester serves as a versatile reagent in chemical synthesis, with applications across multiple fields.

Chloroformylhexanoicacidethylester; 97%

14794-32-2: 6-(Chloroformyl)hexanoic acid ethyl ester, Ethyl 7-Chloro-7-Oxoheptanoate

Ethyl 6-(Chloroformyl)hexanoate

Ethyl 6-(chloroformyl)hexanoate

Heptanoic acid, 7-chloro-7-oxo-, ethyl ester

Ethyl 6-(Chloroformyl)Hexanoate

Ethyl 6-(Chloroformyl)hexanoate is a thiolate that reacts with metals to form metal thiolates. It is used as an additive in ceramic glazes and as a catalyst for organic synthesis.

CAS 14794-32-2: Chloroformylhexanoicacidethylester; 97%

Ethyl 6-(Chloroformyl)hexanoate

Ref: 3B-C1414

Ethyl 6-(chloroformyl)hexanoate

Ref: 10-F011332

Heptanoic acid, 7-chloro-7-oxo-, ethyl ester

Ref: IN-DA001FBP

Ethyl 6-(Chloroformyl)Hexanoate

Ref: 54-OR1027352

Ethyl 6-(Chloroformyl)hexanoate

Ref: 3D-PAA79432