Skip to Content
MilliporeSigma
All Photos(2)

Key Documents

16503

Sigma-Aldrich

Methyl 2-bromo-2-butenoate

(cis+trans), ≥95.0% (GC)

Synonym(s):

Methyl 2-bromocrotonate

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
CH3CH=CBrCOOCH3
CAS Number:
Molecular Weight:
179.01
Beilstein:
1700999
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

≥95.0% (GC)

refractive index

n20/D 1.486

bp

178-182 °C (lit.)

density

1.505 g/mL at 20 °C (lit.)

functional group

bromo
ester

storage temp.

2-8°C

SMILES string

COC(=O)C(Br)=CC

InChI

1S/C5H7BrO2/c1-3-4(6)5(7)8-2/h3H,1-2H3

InChI key

DMKWWKUPZZAUQL-UHFFFAOYSA-N

General description

Methyl 2-bromo-2-butenoate(Methyl (Z)-2-bromocrotonate) yields (S)-2-bromobutanoic acid by baker′s yeast fermentation. It undergoes biotransformation catalyzed by old yellow enzyme to yield methyl (S)-2-bromobutanoate, a key intermediate for the synthesis of chiral drugs. It is a biannelating reagent which participates in double Michael-additions.

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)

145.4 °F - closed cup

Flash Point(C)

63 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

H. Hagiwara et al.
Journal of the Chemical Society. Chemical Communications, 413-413 (1976)
Enoate reductase-mediated preparation of methyl (S)-2-bromobutanoate, a useful key intermediate for the synthesis of chiral active pharmaceutical ingredients.
Brenna E, et al.
Organic Process Research & Development, 16(2), 262-268 (2011)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service