143806-23-9

Basic information

• Product Name: 3-Pyridinecarboxylic acid, 6-methyl-4-phenyl-, methyl ester
• CAS NO: 143806-23-9
• Molecular Formula: C14H13NO2
• Molecular Weight: 227.263
• Mol File: 143806-23-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 3-Pyridinecarboxylic acid, 6-methyl-4-phenyl-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Pyridinecarboxylic acid, 6-methyl-4-phenyl-, methyl ester(143806-23-9)
• EPA Substance Registry System: 3-Pyridinecarboxylic acid, 6-methyl-4-phenyl-, methyl ester(143806-23-9)

Safety Data

• Hazardous Substances Data: 143806-23-9(Hazardous Substances Data)

Usage

General Description

3-Pyridinecarboxylic acid, 6-methyl-4-phenyl-, methyl ester is a chemical compound that is a derivative of pyridinecarboxylic acid. It is also known as methyl 6-methyl-4-phenyl-3-pyridinecarboxylate. 3-Pyridinecarboxylic acid, 6-methyl-4-phenyl-, methyl ester has potential applications in the pharmaceutical industry, particularly for its properties as a potential inhibitor of enzymes related to diseases such as Alzheimer's and Parkinson's. It may also have uses in the field of organic synthesis for the production of various other compounds. Overall, this chemical compound has potential utility in both the pharmaceutical and industrial sectors.

Upstream product

• 132819-55-7 2-Methyl-4-phenyl-4H-pyridine-1-carboxylic acid ethyl ester 
• 1060805-95-9 4-chloro-6-methylnicotinic acid 
• 886372-05-0 methyl 4-chloro-6-methylpyridine-3-carboxylate 
• 98-80-6 phenylboronic acid 
• 88459-86-3 3-Methyl-5-phenyl-isotellurazole 
• 922-67-8 propynoic acid methyl ester 
• 5470-70-2 Methyl 6-methylnicotinate 

Relevant articles and documents

Five-membered azole heterocyclic compound and its preparation method, pharmaceutical composition and use thereof

The present invention relates to a five-membered azole heterocycle compound represented by the following general formula (I), a preparation method of the five-membered azole heterocycle compound, a drug composition of the five-membered azole heterocycle compound, and a use of the five-membered azole heterocycle compound in preparation of drugs for prevention or treatment of TGR5-mediated diseases. The formula (I) is represented by the instruction.

Regioselective synthesis of polysubstituted pyridines via hetero-Diels-Alder reaction of isotellurazoles with acetylenic dienophiles

Treatment of substituted isotellurazoles or their Te-oxides with acetylenic dienophiles efficiently afforded polysubstituted pyridine derivatives through a pathway involving hetero-Diels-Alder reaction of isotellurazoles and the subsequent tellurium extru

Regioselective Addition ofd Copper-Zinc Aryl Organometallic Reagents to 3-substituted Pyridinium Salts

A number of 3-substituted pyridinium salts are subjected to nucleophilic addition by copper-zinc aryl organometallic reagents.The adducts are oxidized subsequently to form the corresponding 4-arylpyridines.In all the cases 1,4-addition products are obtained predominantly.The regioselectivity can be rationalized according to the hard-soft acid-base principle.Calculations on both charge distributions and FMO coefficients indicate that these reactions may be classified on the basis of the type of soft acid-soft base reactions.The observed γ-attack complies very well with the orientation of the FMO coefficients as estimated by a semiempirical method.