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Bicyclo[4.2.0]octa-1,3,5-triene, 7,8-diphenyl-, cis- is a complex organic compound with the molecular formula C16H14. It is a bicyclic molecule, featuring a cycloalkene structure with two phenyl groups attached to the 7th and 8th carbon atoms. The cis-configuration indicates that the two phenyl groups are positioned on the same side of the molecule. Bicyclo[4.2.0]octa-1,3,5-triene, 7,8-diphenyl-, cis- is known for its unique geometric isomerism and is often studied in the context of organic chemistry due to its interesting structural properties and potential applications in the synthesis of other organic compounds.

6894-86-6

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6894-86-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6894-86-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,9 and 4 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6894-86:
(6*6)+(5*8)+(4*9)+(3*4)+(2*8)+(1*6)=146
146 % 10 = 6
So 6894-86-6 is a valid CAS Registry Number.

6894-86-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (7R,8S)-7,8-diphenylbicyclo[4.2.0]octa-1,3,5-triene

1.2 Other means of identification

Product number -
Other names Bicyclo[4.2.0]octa-1,3,5-triene,7,8-diphenyl-,cis

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:6894-86-6 SDS

6894-86-6Relevant academic research and scientific papers

Reaction of trialkyl(dibromomethyl)silanes or 1,2-bis(dibromomethyl)benzene with triorganomanganates. A facile and selective synthesis of alkenylsilanes and 1,2-diaryl-1,2-dihydrobenzocyclobutenes

Kakiya,Shinokubo,Oshima

, p. 2139 - 2147 (2007/10/03)

Treatment of trialkyl(dibromomethyl)silanes with trialkylmanganates, derived from manganese(II) chloride and three molar amounts of Grignard reagents or alkyllithiums, provided (E)-1-trialkylsilyl-1-alkenes with high stereoselectivity in good yields. The reaction of trialkyl(dibromomethyl)silanes with alkylmagnesium halides proceeded in the presence of a catalytic amount of manganese(II) chloride. Treatment of 1,2-bis(dibromomethyl)benzene with triphenylmanganate gave 1,2-diphenyl-1,2-dihydrobenzocyclobutene.

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