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1-(cyclopent-1-en-1-ylsulfonyl)-4-methylbenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

67963-04-6

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67963-04-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67963-04-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,9,6 and 3 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 67963-04:
(7*6)+(6*7)+(5*9)+(4*6)+(3*3)+(2*0)+(1*4)=166
166 % 10 = 6
So 67963-04-6 is a valid CAS Registry Number.

67963-04-6Relevant articles and documents

BORON-CONTAINING CYCLIC EMISSIVE COMPOUNDS AND COLOR CONVERSION FILM CONTAINING THE SAME

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Page/Page column 113, (2020/10/21)

The present disclosure relates to novel photoluminescent complexes comprising a BODIPY moiety covalently bonded to a blue light absorbing moiety, a color conversion film comprising the photoluminescent complex, and a back-light unit using the same.

HEPATITIS C VIRUS INHIBITORS AND USES THEREOF IN PREPARATION OF DRUGS

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, (2017/12/17)

A series of hepatitis C virus (HCV) inhibitors and compositions and applications thereof in the preparation of drugs for treating chronic HCV infection. Especially, a series of compounds that are used as NS5A inhibitors, and compositions and uses thereof in the preparations of drugs.

Discovery and evaluation of Cav3.2-selective T-type calcium channel blockers

Bezen?on, Olivier,Remeň, Lubo?,Richard, Sylvia,Roch, Catherine,Kessler, Melanie,Ertel, Eric A.,Moon, Richard,Mawet, Jacques,Pfeifer, Thomas,Capeleto, Bruno

, p. 5326 - 5331 (2017/10/30)

We identified and characterized a series of pyrrole amides as potent, selective Cav3.2-blockers. This series culminated with the identification of pyrrole amides 13b and 26d, with excellent potencies and/or selectivities toward the Cav3.1- and Cav3.3-channels. These compounds display poor physicochemical and DMPK properties, making their use difficult for in vivo applications. Nevertheless, they are well-suited for in vitro studies.

Polystyrene-supported selenosulfonates: Efficient reagents for regio- and stereocontrolled synthesis of vinyl sulfones

Qian,Huang

, p. 1913 - 1916 (2007/10/03)

Two novel polystyrene-supported selenosulfonates reagents have been developed. As reagents for boron trifluoride catalyzed or AIBN catalyzed addition to olefins were successfully demonstrated and have been used for regioselective synthesis of vinyl sulfon

Preparation and Stereochemistry of Methylation of Some Cycloalkyl Sulfones

Rothberg, Irvin,Sundoro, Boby,Balanikas, George,Kirsch, Sheldon

, p. 4345 - 4348 (2007/10/02)

3-((4-methylphenyl)sulfonyl)cyclohexanols (2, 3), 3-((4-methylphenyl)sulfonyl)cyclopentanols (7, 8), and 2-((4-methylphenyl)sulfonyl)cyclopentanols (12, 15) and their tetrahydropyranyl ether derivatives were prepared.Attempted methylation of the tetrahydr

Copper-Catalyzed Additions of Sulfonyl Iodides to Simple and Cyclic Alkenes

Liu, Lilian Kao,Chi, Y.,Jen, Kwan-Yue

, p. 406 - 410 (2007/10/02)

A convenient synthesis for various β-iodo sulfones has been developed.The reaction involves additions of alkane- and arenesulfonyl iodides to simple and cyclic alkenes under the catalytic action of copper(II) chloride.The favored stereochemical results for cyclic alkenes have been rationalized in terms of stepwise addition of both portions of the addend from the diaxial direction.

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