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590-15-8

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590-15-8 Usage

Uses

trans -1-Bromo-1-propene is suitable for the synthesis of (E)-hex-4-en-2-yn-1-ol. trans -1-Bromo-1-propene ((E)-1-bromo-1-propene) may be used in the synthesis of the following:(E)-1,3-dimethyl-3-(prop-1-enyl)indolin-2-one3-alkenyl-Δ3-cephems(E)-1-(benzylthio)-1-propene

General Description

trans-1-Bromo-1-propene is an alkenyl halide. Product contains copper as stabilizer. Its synthesis from 1,2-dibromopropane has been reported by various researchers. Its IR spectra has been investigated.

Check Digit Verification of cas no

The CAS Registry Mumber 590-15-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,9 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 590-15:
(5*5)+(4*9)+(3*0)+(2*1)+(1*5)=68
68 % 10 = 8
So 590-15-8 is a valid CAS Registry Number.
InChI:InChI=1S/C3H5Br/c1-2-3-4/h2-3H,1H3/b3-2+

590-15-8 Well-known Company Product Price

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  • Aldrich

  • (391107)  trans-1-Bromo-1-propene  contains copper as stabilizer, 99%

  • 590-15-8

  • 391107-1G

  • 611.91CNY

  • Detail
  • Aldrich

  • (391107)  trans-1-Bromo-1-propene  contains copper as stabilizer, 99%

  • 590-15-8

  • 391107-5G

  • 2,093.13CNY

  • Detail

590-15-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-BROMO-1-PROPENE

1.2 Other means of identification

Product number -
Other names trans-1-bromoprop-1-ene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:590-15-8 SDS

590-15-8Relevant articles and documents

A novel system for decarboxylative bromination

Telvekar, Vikas N.,Chettiar, Somsundaram N.

, p. 4529 - 4532 (2008/02/03)

A simple and mild method for decarboxylative bromination of α,β-unsaturated carboxylic acids has been developed using diphosphorus tetraiodide in combination with tetraethylammonium bromide (TEAB) at room temperature. High yields of the corresponding bromoalkenes were obtained.

Synthesis of the Substituted Z-1-Bromo-1-alkenes and Arylacetylenes from 2,3-Dibromocarboxylic Acids

Matveeva,Erin,Kurz

, p. 1065 - 1067 (2007/10/03)

Stereoselectivity was studied of simultaneous debromination-decarboxylation of dibrominated cinnamic and acrylic acids. The best selectivity in formation of Z-vinyl bromides was achieved with the use of organic nitrogen bases. The 1-bromo-1-alkenes were converted into the corresponding acetylenes.

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