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Benzene, 1,1'-(2,3-dimethyl-2-butene-1,4-diyl)bis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73807-73-5

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73807-73-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73807-73-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,8,0 and 7 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 73807-73:
(7*7)+(6*3)+(5*8)+(4*0)+(3*7)+(2*7)+(1*3)=145
145 % 10 = 5
So 73807-73-5 is a valid CAS Registry Number.

73807-73-5SDS

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 (2,3-dimethylbut-2-ene-1,4-diyl)dibenzene

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:73807-73-5 SDS

73807-73-5Downstream Products

73807-73-5Relevant academic research and scientific papers

Stereoselective hydrogenations of aryl-substituted dienes

Cui, Xiuhua,Ogle, James W.,Burgess, Kevin

, p. 672 - 674 (2005)

The carbene complex 1 can mediate hydrogenations of dienes with up to 20:1.0 diastereoselectivity and 99% ee; the scope and limitations of these reactions were investigated. The Royal Society of Chemistry 2005.

Photochemical Addition of Benzyltriethylgermane and Dibenzyldiethylgermane to Olefines

Kobayashi, Masanori,Yoshida, Masato,Kobayashi, Michio

, p. 3169 - 3174 (2007/10/02)

A novel photochemical addition of a germanyl radical to the olefinic double bond was discovered when benzyltriethylgermane or dibenzyldiethylgermane was irradiated with a medium-pressure mercury lamp in the presence of olefins.

AN OLEFIN POLYANION EQUIVALENT: A NEW OLEFIN SYNTHESIS FROM TRIFLONES

Hendrickson, James B.,Boudreaux, Gerald J.,Palumbo, Paul S.

, p. 4617 - 4618 (2007/10/02)

α-Trifyl-dimethylsulfone (CF3SO2CH2SO2CH3) is a reagent which allows successive polyalkylation of the two carbons with regiocontrol.The polyalkylated trifyl-sulfone then undergoes a Ramberg-Baecklund reaction with loss of triflinate anion and extrusion of SO2 to form an olefin.In synthetic terms the net structural change is equivalent to regiospecific alkylation of an olefin polyanion, =C==C=.

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