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Benzene, 1,1'-(1E)-1-buten-3-yne-1,4-diylbis[4-iodo- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

833486-09-2

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833486-09-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 833486-09-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,3,3,4,8 and 6 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 833486-09:
(8*8)+(7*3)+(6*3)+(5*4)+(4*8)+(3*6)+(2*0)+(1*9)=182
182 % 10 = 2
So 833486-09-2 is a valid CAS Registry Number.

833486-09-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-4,4'-(but-1-en-3-yne-1,4-diyl)bis(iodobenzene)

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:833486-09-2 SDS

833486-09-2Upstream product

833486-09-2Downstream Products

833486-09-2Relevant academic research and scientific papers

Hydrido-cobalt catalyst as a selective tool for the dimerisation of arylacetylenes: Scope and theoretical studies

Ventre, Sandrine,Derat, Etienne,Amatore, Muriel,Aubert, Corinne,Petit, Marc

supporting information, p. 2584 - 2590 (2013/10/21)

A simple hydrido-cobalt complex efficiently catalyses the highly regio- and stereoselective dimerisation of various terminal arylacetylenes under mild conditions. The corresponding (E)-1,4-enynes are obtained as sole isomers with good to excellent yields. DFT calculations revealed that the reaction proceeds via a C-H activation/hydrocobaltation pathway. Copyright

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