Skip to Content
MilliporeSigma
All Photos(2)

Documents

16505

Sigma-Aldrich

Methyl trans-4-bromo-2-butenoate

technical, ≥90% (GC)

Synonym(s):

Methyl 4-bromocrotonate

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Linear Formula:
BrCH2CH=CHCOOCH3
CAS Number:
6000-00-6
Molecular Weight:
179.01
Beilstein/REAXYS Number:
1745755
MDL number:
MFCD00000246
UNSPSC Code:
12352100
PubChem Substance ID:
57647572
NACRES:
NA.22

grade

technical

assay

≥90% (GC)

contains

silver wool as stabilizer

impurities

~3% methyl cis-4-bromo-2-butenoate

refractive index

n20/D 1.501

bp

70 °C/0.03 mmHg (lit.)

density

1.498 g/mL at 20 °C (lit.)

storage temp.

2-8°C

SMILES string

COC(=O)\C=C\CBr

InChI

1S/C5H7BrO2/c1-8-5(7)3-2-4-6/h2-3H,4H2,1H3/b3-2+

InChI key

RWIKCBHOVNDESJ-NSCUHMNNSA-N

Application

Methyl trans-4-bromo-2-butenoate (Methyl 4-bromocrotonate) was used in the synthesis of highly substituted benzoxepines or benzopyrans and L-α-amino [4,5-3H]adipic acid.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

197.6 °F

flash_point_c

92 °C

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

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

Visit the Document Library

An Allylpalladium (IV) Intermediate in the Synthesis of Highly Substituted Benzoxepines and Benzopyrans via Reactions of Stable Pallada (II) cycles with Allyl Bromides.
Guo R, et al.
Organometallics, 26(15), 3784-3783 (2007)
J O'Sullivan et al.
The Biochemical journal, 184(2), 421-426 (1979-11-15)
1. delta-(L-alpha-Amino[4,5-3H]adipyl)-L-cysteinyl-D-[4,4-3H]valine has been synthesized from its constituent amino acids, the L-alpha-amino[4,5-3H]adipic acid being obtained by reduction with 3H2 of methyl 5-acetamido-5,5-diethoxycarbonylpent-2-enoate and subsequent decarboxylation and hydrolysis. 2. In a cell-free system prepared by lysis of protoplasts of Cephalosporium acremonium

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