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4-chloro-3,4-diphenylcyclopent-2-en-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

93260-12-9

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93260-12-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93260-12-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,2,6 and 0 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 93260-12:
(7*9)+(6*3)+(5*2)+(4*6)+(3*0)+(2*1)+(1*2)=119
119 % 10 = 9
So 93260-12-9 is a valid CAS Registry Number.

93260-12-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-chloro-3,4-diphenylcyclopent-2-en-1-one

1.2 Other means of identification

Product number -
Other names 4-chloro-3,4-diphenylcyclopent-2-enone

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:93260-12-9 SDS

93260-12-9Relevant academic research and scientific papers

The catalytic asymmetric Fischer indolization

Mueller, Steffen,Webber, Matthew J.,List, Benjamin

supporting information; experimental part, p. 18534 - 18537 (2012/01/31)

The first catalytic asymmetric Fischer indolization is reported. In the presence of a 5 mol % loading of a novel spirocyclic chiral phosphoric acid, 4-substituted cyclohexanone-derived phenylhydrazones undergo a highly enantioselective indolization. Efficient catalyst turnover was achieved by the addition of a weakly acidic cation exchange resin, which removes the generated ammonia. The reaction can be conducted under mild conditions and gives various 3-substituted tetrahydrocarbazoles in generally high yields.

Penultimate effect in ethylene-styrene copolymerization and the discovery of highly active ethylene-styrene catalysts with increased styrene reactivity

Arriola, Daniel J.,Bokota, Marilyn,Campbell Jr., Richard E.,Klosin, Jerzy,LaPointe, Robert E.,Redwine, O. David,Shankar, Ravi B.,Timmers, Francis J.,Abboud, Khalil A.

, p. 7065 - 7076 (2008/02/08)

For the first time commercially relevant catalysts for the copolymerization of ethylene and styrene have been identified. The catalysts maintain very high copolymer efficiencies at relatively high reactor temperatures without sacrificing styrene comonomer

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