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408369-24-4

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408369-24-4 Usage

Chemical structure

Benzene derivative with a trifluoromethyl group attached to a phenoxy group and a carbonyl aldehyde functional group

Usage

Commonly used in organic synthesis and pharmaceutical research for its potential pharmacological activities

Applications

Building block in the production of various chemical compounds with diverse applications

Importance

Trifluoromethyl group enhances biological activity and pharmacokinetic properties of drug molecules, making it valuable in drug discovery and development.

Check Digit Verification of cas no

The CAS Registry Mumber 408369-24-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,8,3,6 and 9 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 408369-24:
(8*4)+(7*0)+(6*8)+(5*3)+(4*6)+(3*9)+(2*2)+(1*4)=154
154 % 10 = 4
So 408369-24-4 is a valid CAS Registry Number.

408369-24-4Relevant articles and documents

Metal-free oxidative coupling: Xanthone formation via direct annulation of 2-aryloxybenzaldehyde using tetrabutylammonium bromide as a promoter in aqueous medium

Rao, Honghua,Ma, Xinyi,Liu, Qianzi,Li, Zhongfeng,Cao, Shengli,Li, Chao-Jun

supporting information, p. 2191 - 2196 (2013/10/01)

A metal-free intramolecular annulation of 2-aryloxybenzaldehydes to xanthones is disclosed, which proceeds through the direct oxidative coupling of an aldehyde C-H bond and aromatic C-H bonds using tetrabutylammonium bromide (TBAB) as a promoter in aqueous medium. This strategy works smoothly in the presence of both electron-donating and electron-withdrawing groups, and displays good tolerance towards catalytically reactive substituents, thus promising further functionalizations of xanthone products.

Benzamide compounds as apo b secretion inhibitors

-

, (2008/06/13)

The present invention relates to compounds of the formula (I) wherein R1 and R2 are each independently lower alkyl lower alkenyl, acyl, amino, lower alkoxy, lower cycloalkyloxy, aryl, aryloxy, sulfooxy, mercapto, sulfo, hydrogen, halogen, nitro, cyano or hydroxy, or may form a ring structure; Q1 is N or CH; L is optionally substituted unsaturated 3 to 10-membered heterocyclic group; X is optionally substituted monocyclic arylene or monocyclic heteroarylene; Y is -(A1)m-(A2)n-(A4)k-; Z is directbond, —CH2-, —NH— or —O—; and R is hydrogen or lower alkyl, or a salt thereof The compounds of the present invention inhibit apolipoprotein B (Apo B) secretion and are useful as a medicament for prophylactic and treatment of diseases or conditions resulting from elevated circulating levels of Apo B.

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