85386-20-5

Usage

Uses

Used in Pharmaceutical Industry:
5-Phenylpyrimidine-2-carboxylic acid is used as a building block for the synthesis of various biologically active compounds. Its incorporation into drug molecules can potentially lead to the development of new pharmaceuticals with specific therapeutic effects.
Used in Agrochemical Industry:
In the agrochemical sector, 5-Phenylpyrimidine-2-carboxylic acid is utilized as a precursor in the creation of agrochemicals. Its role in the synthesis of active ingredients can contribute to the development of new pesticides, herbicides, or other agricultural chemicals that enhance crop protection and yield.
For further exploration:
5-Phenylpyrimidine-2-carboxylic acid may also possess untapped biological activities. Further research is necessary to fully understand its properties and potential uses, which could expand its applications beyond the pharmaceutical and agrochemical industries.

Upstream product

• 34771-47-6 2-methyl-5-phenylpyrimidine 
• 37131-87-6 5-bromo-2-pyrimidinecarboxylic acid 
• 98-80-6 phenylboronic acid 
• 31408-20-5 2-(methylthio)-5-phenylpyrimidine 
• 31408-21-6 2-Methylsulfonyl-5-phenylpyrimidine 
• 106307-59-9 2-Tribromomethyl-5-phenylpyrimidine 
• 106307-55-5 2-Styryl-5-phenylpyrimidine 
• 85386-18-1 2-Cyano-5-phenylpyrimidine 

Downstream Products

• 106307-75-9 5-Phenylpyrimidine-2-carboxylic acid chloride 
• 106307-70-4 p-Cyanophenyl p-(5-Phenyl-2-pyrimidylcarbonyloxy)benzoate 
• 106307-74-8 p-(5-Phenyl-2-pyrimidylcarbonyloxy)benzoic acid chloride 
• 106307-71-5 p-(5-Phenyl-2-pyrimidylcarbonyloxy)benzoic acid 
• 106307-65-7 p-Amyloxyphenyl 5-Phenylpyrimidine-2-carboxylate 
• 106307-66-8 p-Cyanophenyl 5-Phenylpyrimidine-2-carboxylate 
• 106307-68-0 p-Amylphenyl p-(5-Phenyl-2-pyrimidylcarbonyloxy)benzoate 
• 106307-64-6 p-Amylphenyl 5-Phenylpyrimidine-2-carboxylate 

Relevant academic research and scientific papers

2-AMINOQUINOLINE DERIVATIVE

This invention provides 2-aminoquinoline derivatives represented by a general formula [I] [in which R1 and R2 either stand for lower alkyl, lower cycloalkyl, etc., or R1 and R2 together form an aliphatic nitroge

IMIDAZOPYRIDINE DERIVATIVES

The invention provides imidazopyridine derivatives represented by the general formula [I] [in which R1 and R2 may be the same or different and stand for C1-6 alkyl or the like, R3 and R4 stand for hydrogen atom, methyl group or the like, W stands for mono- or bi-cyclic 3- to 8-membered aromatic or aliphatic heterocycle or the like, and Ar stands for optionally substituted aromatic heterocycle or the like]. These compounds act as melanin-concentrating hormone receptor antagonist and are useful as medicines for central nervous system disorders, cardiovascular system disorders and metabolic disorders.

CHEMICAL PROPERTIES OF YLIDENE DERIVATIVES OF AZINES. 7. CONVERSIONS OF 5-METHYL(PHENYL)-SUBSTITUTED 1,2-DIHYDRO-2-PYRIMIDINYLIDENEMALONONITRILES BY NITRIC ACID

It has been shown that the reaction of 5-methyl(phenyl)pyrimidinylidenemalononitrile with nitric acid leads either to a 2-pyrimidinecarboxylic acid or to a pyrimidinylidene-α-carboxamido(α-carboxamido, α-nitro)-acetonitrile depending on the conditions.

SYNTHESIS OF 5-ARYLPYRIMIDINE-2-CARBOXYLIC ACIDS AND THE LIQUID-CRYSTAL CHARACTERISTICS OF THEIR ARYL ESTERS

5-Arylpyrimidine-2-carboxylic acids were synthesized by the hydrolysis of 5-aryl-2-cyanopyrimidines and the oxidation of 5-aryl-2-styrylpyrimidines under the conditions of phase-transfer catalysis.The aryl esters of the acids were obtained, and their liqu