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Bicyclo[3.1.0]hex-2-ene, 3,5-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

94995-15-0

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94995-15-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94995-15-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,9,9 and 5 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 94995-15:
(7*9)+(6*4)+(5*9)+(4*9)+(3*5)+(2*1)+(1*5)=190
190 % 10 = 0
So 94995-15-0 is a valid CAS Registry Number.

94995-15-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-diphenylbicyclo[3.1.0]hex-3-ene

1.2 Other means of identification

Product number -
Other names Bicyclo[3.1.0]hex-2-ene,3,5-diphenyl

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:94995-15-0 SDS

94995-15-0Downstream Products

94995-15-0Relevant academic research and scientific papers

Ruthenium- and platinum-catalyzed sequential reactions: Selective synthesis of fused polycyclic compounds from propargylic alcohols and alkenes

Nishibayashi, Yoshiaki,Yoshikawa, Masato,Inada, Youichi,Hidai, Masanobu,Uemura, Sakae

, p. 16066 - 16072 (2007/10/03)

A simple method for the preparation of fused polycyclic compounds by an intramolecular cyclization of propargylic alcohols bearing an alkene moiety at a suitable position has been developed, where the presence of both Ru and Pt catalysts promotes a sequence of catalytic cycles in the same medium. This sequential system can be applied to an intermolecular reaction between a propargylic alcohol and an alkene to obtain the corresponding bicyclo[3,1,0]hex-2-ene derivative. These sequential reactions provide a conceptually new type of cycloaddition system between propargylic alcohols and alkenes.

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