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[1,1'-Biphenyl]-2-carboxylic acid, 6-methyl-4'-(trifluoromethyl)-, methyl ester is a chemical compound with the molecular formula C18H13F3O2. It is a methyl ester derivative of 6-methyl-4'-(trifluoromethyl)-[1,1'-biphenyl]-2-carboxylic acid, characterized by its unique structure and properties.

256397-60-1

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256397-60-1 Usage

Uses

Used in Pharmaceutical Research and Development:
[1,1'-Biphenyl]-2-carboxylic acid, 6-methyl-4'-(trifluoromethyl)-, methyl ester is used as a key intermediate in the synthesis of new drugs and pharmaceutical compounds. Its unique structure allows for the development of novel therapeutic agents with potential applications in various medical fields.
Used in Agrochemicals:
In the agrochemical industry, [1,1'-Biphenyl]-2-carboxylic acid, 6-methyl-4'-(trifluoromethyl)-, methyl ester may be utilized as a component in the development of new pesticides or other agricultural chemicals, contributing to enhanced crop protection and yield.
Used in Material Science:
[1,1'-Biphenyl]-2-carboxylic acid, 6-methyl-4'-(trifluoromethyl)-, methyl
ester's potential applications in material science include its use in the development of advanced materials with specific properties, such as improved stability, reactivity, or selectivity in various chemical processes. Its unique structure and properties make it a promising candidate for further research and development in this field.

Check Digit Verification of cas no

The CAS Registry Mumber 256397-60-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,6,3,9 and 7 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 256397-60:
(8*2)+(7*5)+(6*6)+(5*3)+(4*9)+(3*7)+(2*6)+(1*0)=171
171 % 10 = 1
So 256397-60-1 is a valid CAS Registry Number.

256397-60-1Upstream product

256397-60-1Relevant academic research and scientific papers

Amino-benzocycloalkane derivatives

-

, (2008/06/13)

Compounds of the formula I wherein R2—C, R3—C, R4—C or R5—C may be replaced by N; and wherein n is 1, 2 or 3; R1is aryl, cycloalkyl or heterocyclyl; R2, R3, R4and R5are independently hydrogen, optionally substituted alkyl, halo, amino, substituted amino, trifluoromethyl, cyano, carboxyl, alkoxycarbonyl, aralkoxycarbonyl, (alkyl, aryl or aralkyl)-thio, (alkyl, aryl or aralkyl)-oxy, acyloxy, (alkyl, aryl or aralkyl)-aminocarbonyloxy; or any two of R2, R3, R4and R5at adjacent positions are alkylenedioxy; R6is hydrogen, optionally substituted alkyl, amino, substituted amino, acylamino, wherein Rais hydrogen or optionally substituted alkyl, Rband Rcare independently hydrogen, optionally substituted alkyl, cycloalkyl, aryl or heterocyclyl; or Rband Rctogether represent lower alkylene or lower alkylene interrupted by O, S, or N—(H, alkyl or aralkyl); Rdis optionally substituted alkyl, cycloalkyl, aryl or heterocyclyl; and Reis optionally substituted alkyl, aryl, heterocyclyl, cycloalkyl, amino or substituted amino; and pharmaceutically acceptable salts thereof; and enantiomers thereof; which are useful as inhibitors of microsomal triglyceride transfer protein (MTP) and of apolipoprotein B (ApoB) secretion.

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