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4-methyl-N’-(tetrahydro-4H-thiopyran-4-ylidene)benzenesulfonohydrazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

40697-91-4

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40697-91-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40697-91-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,6,9 and 7 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 40697-91:
(7*4)+(6*0)+(5*6)+(4*9)+(3*7)+(2*9)+(1*1)=134
134 % 10 = 4
So 40697-91-4 is a valid CAS Registry Number.

40697-91-4Relevant academic research and scientific papers

COMPOUNDS USEFUL IN THE TREATMENT OR PREVENTION OF A PRMT5-MEDIATED DISORDER

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Paragraph 00131, (2018/10/19)

The present disclosure relates to compounds suitable for the inhibition of protein arginine methyl-transferase (PRMT), in particular PRMT5. These compounds may be for use as therapeutic agents, in particular, agents for use in the treatment and/or prevent

One-Pot Synthesis of Spirocyclic or Fused Pyrazoles from Cyclic Ketones: Calcium Carbide as the Carbon Source in Ring Expansion

Yu, Yue,Chen, Yang,Huang, Wei,Wu, Wanqing,Jiang, Huanfeng

, p. 9479 - 9486 (2017/09/23)

N-Tosylhydrazones generated in situ from cyclic ketones smoothly underwent a [3 + 2] cycloaddition to afford saturated spirocyclic pyrazoles and further transformed to the fused analogues via a ring expansion in certain cases. An inexpensive and renewable

Metal-free coupling of saturated heterocyclic sulfonylhydrazones with boronic acids

Allwood, Daniel M.,Blakemore, David C.,Brown, Alan D.,Ley, Steven V.

, p. 328 - 338 (2014/01/17)

The coupling of aromatic moieties with saturated heterocyclic partners is currently an area of significant interest for the pharmaceutical industry. Herein, we present a procedure for the metal-free coupling of 4-, 5-, and 6-membered saturated heterocyclic p-methoxyphenyl (PMP) sulfonylhydrazones with aryl and heteroaromatic boronic acids. This procedure enables a simple, two-step synthesis of a range of functionalized sp2-sp3 linked bicyclic building blocks, including oxetanes, piperidines, and azetidines, from their parent ketones.

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