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(2,2-difluro-trans-3-phenyl-1-cyclopropyl)methyl acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

342893-76-9

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342893-76-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 342893-76-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,2,8,9 and 3 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 342893-76:
(8*3)+(7*4)+(6*2)+(5*8)+(4*9)+(3*3)+(2*7)+(1*6)=169
169 % 10 = 9
So 342893-76-9 is a valid CAS Registry Number.

342893-76-9Relevant academic research and scientific papers

Design of fluorinated cyclopropane derivatives of 2-phenylcyclopropylmethylamine leading to identification of a selective serotonin 2C (5-HT2C) receptor agonist without 5-HT2B agonism

Cheng, Jianjun,Kozikowski, Alan P.,McCorvy, John D.,Roth, Bryan L.,Shen, Sida,Zhang, Guiping

, (2019)

A new series of fluorinated 5-HT2C agonists were designed and synthesized on the basis of our previous work on 2-phenylcyclopropylmethylamines as a potential approach for the treatment of central nervous system disorders. Key fluorinated cyclop

Synthesis of gem-difluoromethylene building blocks through regioselective allylation of gem-difluorocyclopropanes

Munemori, Daisuke,Narita, Kent,Nokami, Toshiki,Itoh, Toshiyuki

supporting information, p. 2638 - 2641 (2014/06/09)

gem-Difluorocyclopropane derivatives react with allyltributylstannane in the presence of 2,2′-azobis(isobutyronitrile) to afford 1,6-dienes with a gem-difluoromethylene moiety at the allylic position. The reaction proceeds regioselectively with high yield

RING OPENING REACTION OF gem-DIFLUOROCYCLOPROPYL KETONES WITH NUCLEOPHILES

Kobayashi, Yoshiro,Taguchi, Takeo,Morikawa, Tsutomu,Takase, Toyohiko,Takanashi, Hiroshi

, p. 1047 - 1050 (2007/10/02)

Syntheses of gem-difluorocyclopropyl ketones (3a-d) and their reactions with nucleophiles are described.Ring opening reactions of 3a, c and d with a methanolate and a thiolate anion took entirely different courses of bond scission of the cyclopropane ring.

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