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E14578

Sigma-Aldrich

Ethyl bromopyruvate

technical grade, 90%

Synonym(s):

β-Bromopyruvic acid ethyl ester, 3-Bromo-2-(oxo)propionic acid ethyl ester, 3-Bromo-2-oxopropanoic acid ethyl ester, 3-Bromopyruvic acid ethyl ester, Bromopyruvic acid ethyl ester, Ethyl α-bromopyruvate, Ethyl 3-bromo-2-oxopropanoate, Ethyl 3-bromo-2-oxopropionate, Ethyl 3-bromopyruvate

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About This Item

Linear Formula:
BrCH2COCOOC2H5
CAS Number:
Molecular Weight:
195.01
Beilstein:
1760158
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

grade

technical grade

Quality Level

Assay

90%

refractive index

n20/D 1.469 (lit.)

bp

98-100 °C/10 mmHg (lit.)

density

1.554 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

CCOC(=O)C(=O)CBr

InChI

1S/C5H7BrO3/c1-2-9-5(8)4(7)3-6/h2-3H2,1H3

InChI key

VICYTAYPKBLQFB-UHFFFAOYSA-N

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General description

Ethyl bromopyruvate, also known as Bromopyruvic acid ethyl ester, is an alkyl-substituted α-bromoketones, that is commonly used as a building block in various organic reaction, such as in the synthesis of 1,3-Oxazoline-2-thiones and 3-bromoimidazopyridines.

Application

Ethyl bromopyruvate is used as an electrophile:
  • for the synthesis of thiazoles with substituted benzothioamides
Also, employed in a synthesis of thioxothiazolidines from primary amines and carbon disulfide.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

210.2 °F - closed cup

Flash Point(C)

99 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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N-Methylimidazole-promoted efficient synthesis of functionalized 1, 3-oxazoline-2-thiones under solvent-free conditions
Issa Y, et al.
Synlett, 2008, 1287-1288 (2008)
Chemodivergent synthesis of N-(pyridin-2-yl) amides and 3-bromoimidazo [1, 2-a] pyridines from alpha-bromoketones and 2-aminopyridines
Yanpeng L, et al.
RSC advances, 9, 34671-34676 (2019)
Chin. J. Chem., 24, 381-381 (2006)
Steric and Electronic Factors Influence Regio-isomeric Thiazole Formations Between Substituted Benzothioamides and Ethyl Bromopyruvate
Jun L, et al.
Journal of Heterocyclic Chemistry, 51, 1137-1146 (2014)

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