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368679

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.)

functional group

alkyl halide
bromo

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 1 petroleums
Hazardous rank II
Water insoluble liquid

JAN Code

368679-10G:
368679-VAR:
368679-BULK:
368679-50G:

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Certificates of Analysis (COA)

Lot/Batch Number
MKCP7924
MKCP5117
MKCP5877
MKCK0420
MKCG2206

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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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