Ethyl 4-bromoacetoacetate

CAS Number: 13176-46-0

Molecular Formula: C6H9BrO3

Purity: Ethyl 4-bromoacetoacetate 90% purity

About Ethyl 4-bromoacetoacetate

Ethyl 4-bromo-3-oxobutanoate (CAS 13176-46-0) acts as a high-performance building block in the API intermediates market, where its dual-functional brominated carbonyl structure is essential for the high-precision synthesis of complex heterocyclic scaffolds and antiviral agents. Ethyl 4-bromoacetoacetate (13176-46-0) fu...

Synonyms

Ethyl 4-bromoacetoacetate
13176-46-0
Ethyl 4-bromo-3-oxobutanoate
4-Bromo-3-oxo-butyric acid ethyl ester
Butanoic acid, 4-bromo-3-oxo-, ethyl ester

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Ethyl 4-bromoacetoacetate Specifications

CAS Number

13176-46-0

Molecular Formula

C6H9BrO3

Molecular Weight

209.04 g/mol

IUPAC Name

ethyl 4-bromo-3-oxobutanoate

Canonical SMILES

CCOC(=O)CC(=O)CBr

InChI Key

MGDWUTQKXCZNAJ-UHFFFAOYSA-N

InChI

InChI=1S/C6H9BrO3/c1-2-10-6(9)3-5(8)4-7/h2-4H2,1H3

HSN No

2918300090

CAS Number

13176-46-0

Molecular Formula

C6H9BrO3

Molecular Weight

209.04 g/mol

IUPAC Name

ethyl 4-bromo-3-oxobutanoate

Canonical SMILES

CCOC(=O)CC(=O)CBr

InChI Key

MGDWUTQKXCZNAJ-UHFFFAOYSA-N

InChI

InChI=1S/C6H9BrO3/c1-2-10-6(9)3-5(8)4-7/h2-4H2,1H3

HSN No

2918300090

Molecular Weight

209.04 g/mol

Purity

Ethyl 4-bromoacetoacetate 90% purity

Pharmaceutical Intermediate

An important building block utilized as a reagent for the synthesis of pharmaceuticals, contributing to the development of new drugs and therapeutic agents, particularly antiviral and anti-inflammatory medications

Agrochemical Intermediate

A critical organic intermediate used in the synthesis of agrochemicals, including pesticides and herbicides, to improve chemical effectiveness and selectivity

Fine Chemicals Intermediate

A versatile reagent employed in the production of high-purity chemicals such as fragrances, specialized dyes, and organic pigments

Organic Synthesis Building Block

A functionalized carboxylic acid derivative used in academic and industrial research for constructing complex heterocyclic molecules through reactions like nucleophilic substitution, aldol condensation, and Michael addition.