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Atomfair Ethyl 4-(dimethylamino)butyrate C8H17NO2

Description Ethyl 4-(dimethylamino)butyrate (CAS No. 22041-23-2) is a high-purity organic compound with the molecular formula C8H17NO2. This ester derivative, also known as ethyl 4-(dimethylamino)butanoate, is widely utilized in pharmaceutical research, organic synthesis, and as a precursor for specialty chemicals. Its clear to pale-yellow liquid form and defined molecular weight of 159.23 g/mol ensure consistent performance in reactions. The compound is characterized by its dimethylamino and ester functional groups, making it valuable for nucleophilic substitutions and as a building block in drug discovery. Packaged under inert conditions to maintain stability, it is ideal for researchers requiring precise and reliable reagents.

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Description

Description

Ethyl 4-(dimethylamino)butyrate (CAS No. 22041-23-2) is a high-purity organic compound with the molecular formula C8H17NO2. This ester derivative, also known as ethyl 4-(dimethylamino)butanoate, is widely utilized in pharmaceutical research, organic synthesis, and as a precursor for specialty chemicals. Its clear to pale-yellow liquid form and defined molecular weight of 159.23 g/mol ensure consistent performance in reactions. The compound is characterized by its dimethylamino and ester functional groups, making it valuable for nucleophilic substitutions and as a building block in drug discovery. Packaged under inert conditions to maintain stability, it is ideal for researchers requiring precise and reliable reagents.

  • CAS No: 22041-23-2
  • Molecular Formula: C8H17NO2
  • Molecular Weight: 159.23
  • Exact Mass: 159.125928785
  • Monoisotopic Mass: 159.125928785
  • IUPAC Name: ethyl 4-(dimethylamino)butanoate
  • SMILES: CCOC(=O)CCCN(C)C
  • Synonyms: Ethyl 4-(dimethylamino)butanoate, 22041-23-2, Ethyl 4-(dimethylamino)butyrate, Butanoic acid, 4-(dimethylamino)-, ethyl ester, KL1P3VC64F

Application

Ethyl 4-(dimethylamino)butyrate serves as a versatile intermediate in the synthesis of pharmaceuticals, particularly for compounds targeting neurological and cardiovascular applications. Its reactive ester group facilitates coupling reactions, while the dimethylamino moiety enhances solubility and bioavailability in drug formulations. Researchers also employ it in the development of chiral auxiliaries and as a ligand modifier in catalytic systems. Additionally, it finds use in agrochemical research for designing novel active ingredients.

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