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130955-17-8

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130955-17-8 Usage

Molecular Weight

207.1 g/mol

Physical State

Clear, colorless liquid

Purity Level

97%

Family

Alkene compounds

Uses

Synthesis of pharmaceuticals
Synthesis of agrochemicals
Production of organic compounds
Chemical intermediate in dye production
Chemical intermediate in perfume production
Chemical intermediate in flavor production

Check Digit Verification of cas no

The CAS Registry Mumber 130955-17-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,9,5 and 5 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 130955-17:
(8*1)+(7*3)+(6*0)+(5*9)+(4*5)+(3*5)+(2*1)+(1*7)=118
118 % 10 = 8
So 130955-17-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H13Br/c1-9(2)7-8-10-5-3-4-6-11(10)12/h3-6H,1,7-8H2,2H3

130955-17-8 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Aldrich

  • (633585)  4-(2-Bromophenyl)-2-methyl-1-butene  97%

  • 130955-17-8

  • 633585-1G

  • 1,473.03CNY

  • Detail

130955-17-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-bromo-2-(3-methylbut-3-enyl)benzene

1.2 Other means of identification

Product number -
Other names -

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:130955-17-8 SDS

130955-17-8Relevant articles and documents

Iridium(I)-Catalyzed Intramolecular Hydrocarbonation of Alkenes: Efficient Access to Cyclic Systems Bearing Quaternary Stereocenters

Fernández, David F.,Gulías, Moisés,Mascare?as, José L.,López, Fernando

supporting information, p. 9541 - 9545 (2017/08/01)

A catalytic, versatile and atom-economical C?H functionalization process that provides a wide variety of cyclic systems featuring methyl-substituted quaternary stereocenters is described. The method relies on the use of a cationic IrI–bisphosph

Asymmetric synthesis of medium-sized rings by intramolecular au(I)-catalyzed cyclopropanation

Watson, Iain D. G.,Ritter, Stefanie,Toste, F. Dean

supporting information; experimental part, p. 2056 - 2057 (2009/07/30)

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