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Sigma-Aldrich

cis-1-Bromo-1-propene

97%

Synonym(s):

(Z)-1-Bromo-1-propene, (Z)-1-Bromoprop-1-ene, (Z)-1-Bromopropene, (Z)-1-Propenyl bromide, (Z)-Propenyl bromide, cis-1-Bromopropene, cis-1-Propenyl bromide

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About This Item

Linear Formula:
CH3CH=CHBr
CAS Number:
590-13-6
Molecular Weight:
120.98
MDL number:
MFCD00082571
UNSPSC Code:
12352100
PubChem Substance ID:
24862924
NACRES:
NA.22

Quality Level

100

Assay

97%

form

liquid

contains

copper as stabilizer

refractive index

n20/D 1.4545 (lit.)

bp

58 °C (lit.)

density

1.423 g/mL at 25 °C (lit.)

SMILES string

C\C=C/Br

InChI

1S/C3H5Br/c1-2-3-4/h2-3H,1H3/b3-2-

InChI key

NNQDMQVWOWCVEM-IHWYPQMZSA-N

Related Categories

General description

cis-1-Bromo-1-propene is an aliphatic olefin. Oxidation of cis-1-bromo-1-propene by toluene dioxygenase has been reported.

Application

cis-1-Bromo-1-propene is used in the preparation of (Z)-1-lithio-1-propeneusing lithium powder.

accessory

Product No.
Description
Pricing

Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Danger

Hazard Statements

H225 - H315 - H319 - H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

-29.2 °F - closed cup

Flash Point(C)

-34 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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’.

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Stereoselective synthesis of a functionalized 2-oxo-1-azabicyclo [5.3. 0] alkane as a potential scaffold for targeted chemotherapy strategies
Bracci A, et al.
Synthesis, 15, 2363-2367 (2003)
C C Lange et al.
Journal of bacteriology, 179(12), 3858-3865 (1997-06-01)
Toluene dioxygenase from Pseudomonas putida F1 has been studied extensively with aromatic substrates. The present work examined the toluene dioxygenase-catalyzed oxidation of various halogenated ethenes, propenes, butenes and nonhalogenated cis-2-pentene, an isomeric mix of 2-hexenes, cis-2-heptene, and cis-2-octene as substrates

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