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8H-Cyclohepta[b]naphthalene, 5,11-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

95895-30-0

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95895-30-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95895-30-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,8,9 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 95895-30:
(7*9)+(6*5)+(5*8)+(4*9)+(3*5)+(2*3)+(1*0)=190
190 % 10 = 0
So 95895-30-0 is a valid CAS Registry Number.

95895-30-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,11-diphenyl-8H-cyclohepta[b]naphthalene

1.2 Other means of identification

Product number -
Other names 5,11-Diphenyl-8H-cyclohepta<b>naphthalin

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:95895-30-0 SDS

95895-30-0Downstream Products

95895-30-0Relevant academic research and scientific papers

On the Chemistry of Some - and Propellanes

Baumgart, Klaus-Dieter,Harnisch, Hanna,Szeimies-Seebach, Ursula,Szeimies, Guenter

, p. 2883 - 2916 (2007/10/02)

On heating the propellanes 2a and b and the propellanes 3, 4a - c, 5, and 6 were isomerized to the 1,3-dienes 7, 10, 11, 12, and 13.The rates of these rearrangements were strongly enhanced by traces of unknown electrophilic reagents.Addition

SKATTEBOL TYPE REARRANGEMENT VIA α-BROMOTRIMETHYLSTANNYL CYCLOPROPANE THERMOLYSIS. WHAT IS THE MECHANISM?

Warner, Philip M.,Herold, Robert D.

, p. 4897 - 4900 (2007/10/02)

Solution thermolysis of the epimers 5 gave rise to separate sets of products, including, for one, Skattebol-type rearrangement.However, neither epimer produced a free carbene.

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