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2,5-Cyclohexadien-1-one, 2-chloro-4-(2,4,6-cycloheptatrien-1-ylidene)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89745-97-1

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89745-97-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89745-97-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,7,4 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 89745-97:
(7*8)+(6*9)+(5*7)+(4*4)+(3*5)+(2*9)+(1*7)=201
201 % 10 = 1
So 89745-97-1 is a valid CAS Registry Number.

89745-97-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-4-cyclohepta-2,4,6-trien-1-ylidenecyclohexa-2,5-dien-1-one

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:89745-97-1 SDS

89745-97-1Upstream product

89745-97-1Downstream Products

89745-97-1Relevant academic research and scientific papers

ELECTRONIC STRUCTURE AND KINETIC BEHAVIOR OF 4-(CYCLOHEPTATRIENYLIDENE)CYCLOHEXA-2,5-DIENONE (OR QUINAREN-9-ONE) AND ITS DERIVATIVES

Takahashi, Kazuko,Nozoe, Tetsuo,Takase, Kahei,Kudo,Toshiaki

, p. 77 - 80 (1984)

The conjugative interaction between the two terminal groups in title quinarenone 2 and its chloro- and methoxy-derivatives were evaluated, proving that the diatropicity of the seven-membered ring is a little larger in 2 than in tropone.Some of these quinarenones are also found to exist in equilibrium with their oligomers and show unexpectedly low barriers of rotation about the intercyclic bond.

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