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(S)-3-(4-chlorophenylthio)-cyclohexanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84658-21-9

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84658-21-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84658-21-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,6,5 and 8 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 84658-21:
(7*8)+(6*4)+(5*6)+(4*5)+(3*8)+(2*2)+(1*1)=159
159 % 10 = 9
So 84658-21-9 is a valid CAS Registry Number.

84658-21-9Downstream Products

84658-21-9Relevant academic research and scientific papers

Highly enantioselective organocatalytic sulfa-michael addition to α, β-unsaturated ketones

Rana, Nirmal K.,Selvakumar, Sermadurai,Singh, Vinod K.

supporting information; experimental part, p. 2089 - 2091 (2010/06/16)

"Chemical Equation Presented" A cinchona alkaloid-derived urea was found to be an efficient organocatalyst for catalyzing enantioselective conjugate addition between thiols and various α,β-unsaturated ketones to provide optically active sulfides with high

Asymmetrie ruthenium-catalyzed 1,4-additions of aryl thiols to enones

Badoiu, Andrei,Bernardinelli, Gerald,Besnard, Celine,Peter Kuendig

supporting information; experimental part, p. 193 - 200 (2010/04/25)

Well defined, stable, one-point binding ruthenium complexes 1 and 2 selectively bind and activate α,β-unsaturated carbonyl compounds for cycloaddition reactions. These mild Lewis acids catalyze asymmetric 1,4-addition reactions of aryl thiols to enones wi

Synthesis and resolution of a multifunctional inherently chiral calix[4]arene with an ABCD substitution pattern at the wide rim: The effect of a multifunctional structure in the organocatalyst on enantioselectivity in asymmetric reactions

Shirakawa, Seiji,Kimura, Tomohiro,Murata, Shun-Ichi,Shimizu, Shoichi

experimental part, p. 1288 - 1296 (2009/06/28)

An efficient synthetic route to inherently chiral calix[4]arenes with an ABCD substitution pattern at the wide rim in the cone conformation was developed for the first time. For the synthesis of inherently chiral ABCD-type calix[4]arenes, first 5,11-dibro

Addition of Aromatic Thiols to Conjugated Cycloalkenones, Catalyzed by Chiral β-Hydroxy Amines. A Mechanistic Study on Homogeneous Catalytic Asymmetric Synthesis

Hiemstra, Henk,Wynberg, Hans

, p. 417 - 430 (2007/10/02)

Reactions between aromatic thiols and conjugated cycloalkenones afford optically active 3-arylthiocycloalkanones, when chiral bases are used as catalysts.This paper reports a detailed investigation into the mechanism of this catalytic asymmetric synthesis

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