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(3-fluoro-4-methoxyphenyl)(phenyl)methanone is a chemical compound with the molecular formula C15H11FO2. It is a derivative of benzophenone, featuring a fluorine atom at the 3-position and a methoxy group at the 4-position of one phenyl ring. (3-fluoro-4-methoxyphenyl)(phenyl)methanone is an aromatic ketone, characterized by the presence of a carbonyl group (C=O) between the two phenyl rings. It is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds due to its unique electronic properties conferred by the fluorine and methoxy substituents. The compound's structure allows for various chemical reactions, such as nucleophilic aromatic substitution, making it a versatile building block in organic chemistry.

345-68-6

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345-68-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 345-68-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,4 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 345-68:
(5*3)+(4*4)+(3*5)+(2*6)+(1*8)=66
66 % 10 = 6
So 345-68-6 is a valid CAS Registry Number.

345-68-6Relevant academic research and scientific papers

MODULATORS OF HSD17B13 AND METHODS OF USE THEREOF

-

, (2021/01/23)

The disclosure relates to compounds and pharmaceutical compositions capable of modulating the hydroxysteroid 17-beta dehydrogenase (HSD17B) family member proteins including inhibiting the HSD17B member proteins, e.g. HSD17B13. The disclosure further relates to methods of treating liver diseases, disorders, or conditions with the compounds and pharmaceutical compositions disclosed herein, in which the HSD17B family member protein plays a role.

Esters as acylating reagent in a Friedel-Crafts reaction: Indium tribromide catalyzed acylation of arenes using dimethylchlorosilane

Nishimoto, Yoshihiro,Babu, Srinivasarao Arulananda,Yasuda, Makoto,Baba, Akio

supporting information; experimental part, p. 9465 - 9468 (2009/04/06)

(Chemical Equation Presented) The Friedel-Crafts acylation of arenes with esters by dimethylchlorosilane and 10 mol % of indium tribromide has been achieved. The key intermediate RCOOSi(Cl)Me2 is generated from alkoxy esters with the evolution of the corresponding alkanes. The scope of the alkoxy ester moiety was wide: tert-butyl, benzyl, allyl, and isopropyl esters were successful. In addition, we demonstrated the direct synthesis of the indanone intermediate 11 of salviasperanol from ester 10.

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