Diethyl bromo(ethyl)propanedioate, with the CAS number 29237-78-3, is an organic compound that belongs to the class of diesters. It features a bromo substituent on one of its ethyl groups, which contributes to its reactivity and potential applications in organic synthesis. The compound typically exhibits a colorless to pale yellow liquid form, characterized by a fruity or sweet odor. Its structure includes two ethyl ester groups attached to a propanedioate backbone, making it a versatile intermediate in various chemical reactions, particularly in the synthesis of more complex molecules. The presence of the bromine atom enhances its electrophilic character, allowing it to participate in nucleophilic substitution reactions. Additionally, diethyl bromo(ethyl)propanedioate is soluble in organic solvents, which facilitates its use in laboratory settings. Safety precautions should be observed when handling this compound, as it may pose health risks if inhaled or ingested. Overall, its unique structure and reactivity make it a valuable compound in synthetic organic chemistry.

diethyl bromo(ethyl)propanedioate

29237-78-3: Diethyl bromo(ethyl)propanedioate, with the CAS number 29237-78-3, is an organic compound that belongs to the class of diesters. It features a bromo substituent on one of its ethyl groups, which contributes to its reactivity and potential applications in organic synthesis. The compound typically exhibits a colorless to pale yellow liquid form, characterized by a fruity or sweet odor. Its structure includes two ethyl ester groups attached to a propanedioate backbone, making it a versatile intermediate in various chemical reactions, particularly in the synthesis of more complex molecules. The presence of the bromine atom enhances its electrophilic character, allowing it to participate in nucleophilic substitution reactions. Additionally, diethyl bromo(ethyl)propanedioate is soluble in organic solvents, which facilitates its use in laboratory settings. Safety precautions should be observed when handling this compound, as it may pose health risks if inhaled or ingested. Overall, its unique structure and reactivity make it a valuable compound in synthetic organic chemistry.

CAS 29237-78-3

diethyl bromo(ethyl)propanedioate

Propanedioic acid, 2-bromo-2-ethyl-, 1,3-diethyl ester

Ref: IN-DA002XSO

Diethyl-(2-bromoethyl)malonate

Ref: 54-OR1321