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(S)-3-methyl-4,4-bis(phenylsulfonyl)butanal is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1201829-82-4

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1201829-82-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1201829-82-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,1,8,2 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1201829-82:
(9*1)+(8*2)+(7*0)+(6*1)+(5*8)+(4*2)+(3*9)+(2*8)+(1*2)=124
124 % 10 = 4
So 1201829-82-4 is a valid CAS Registry Number.

1201829-82-4Downstream Products

1201829-82-4Relevant academic research and scientific papers

A theoretical and experimental study of the effects of silyl substituents in enantioselective reactions catalyzed by diphenylprolinol silyl ether

Hayashi, Yujiro,Okamura, Daichi,Yamazaki, Tatsuya,Ameda, Yasuto,Gotoh, Hiroaki,Tsuzuki, Seiji,Uchimaru, Tadafumi,Seebach, Dieter

supporting information, p. 17077 - 17088 (2015/02/19)

The effect of silyl substituents in diphenylprolinol silyl ether catalysts was investigated. Mechanistically, reactions catalyzed by diphenylprolinol silyl ether can be categorized into three types: two that involve an iminium ion intermediate, such as fo

The organocatalytic addition of bis(arylsulfonyl)methane to α,β-unsaturated aldehydes and the synthesis of optically-enriched 3-methyl-alkanols

Garcia Ruano, Jose Luis,Marcos, Vanesa,Aleman, Jose

supporting information; experimental part, p. 4435 - 4437 (2009/12/29)

An indirect organocatalytic method for the β-methylation of α,β-unsaturated aldehydes that involves the addition of bis(arylsulfonyl)methane catalyzed by prolinol derivatives and further elimination of the chameleonic sulfonyl groups is presented. The Roy

Formal highly enantioselective organocatalytic addition of alkyl anions to α,β-unsaturated aldehydes: Application to the synthesis of isotope-enantiomers

Alba, Andrea-Nekane,Companyo, Xavier,Moyano, Albert,Rios, Ramon

supporting information; scheme or table, p. 11095 - 11099 (2010/04/26)

A practical and powerful methodology that constitutes an organocatalytic alternative for organometallic 1,4-additions was developed. In a vial, bis(phenylsulfonyl)methane and catalyst V were added to toluene. Next, unsaturated aldehyde 1a was added and th

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