126179-78-0

Basic information

• Product Name: methyl3-(pyridin-4-yl)benzoate
• Synonyms: methyl3-(pyridin-4-yl)benzoate;Benzoic acid, 3-(4-pyridinyl)-, methyl ester;Methyl 3-(4-Pyridinyl)Benzoate(WX618344)
• CAS NO: 126179-78-0
• Molecular Formula: C₁₃H₁₁NO₂
• Molecular Weight: 213.23194
• Mol File: 126179-78-0.mol

Chemical Properties

• Boiling Point: 356.8±25.0 °C(Predicted)
• Appearance: /
• Density: 1.147±0.06 g/cm3(Predicted)
• PKA: 4.76±0.26(Predicted)
• CAS DataBase Reference: methyl3-(pyridin-4-yl)benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl3-(pyridin-4-yl)benzoate(126179-78-0)
• EPA Substance Registry System: methyl3-(pyridin-4-yl)benzoate(126179-78-0)

Safety Data

• Hazardous Substances Data: 126179-78-0(Hazardous Substances Data)

Upstream product

• 93-58-3 benzoic acid methyl ester 
• 15854-87-2 4-iodopyridine 
• 618-89-3 methyl 3-bromobenzoate 
• 1692-15-5 4-pyridylboronic acid 

Downstream Products

• 478375-05-2 1-oxy-4-[3-(methoxycarbonyl)phenyl]pyridium 

Relevant articles and documents

CARBOXYLIC ACID DERIVATIVE AND MEDICINE COMPRISING SALT OR ESTER OF THE SAME

The present invention provides novel carboxylic acid derivatives useful as an insulin sensitizer, a salt thereof or a hydrate of them, and a medicament comprising the derivative as the active ingredient. Specifically, it provides a carboxylic acid derivative represented by the following formula: (wherein L represents a single bond, or a C1 to C6 alkylene group, a C2 to C6 alkenylene group or a C2 to C6 alkynylene group, each of which may have one or more substituent groups; M represents a single bond, or a C1 to C6 alkylene group, a C2 to C6 alkenylene group or a C2 to C6 alkynylene group, each of which may have one or more substituent groups; T represents a single bond, or a C1 to C3 alkylene group, a C2 to C3 alkenylene group or a C2 to C3 alkynylene group, each of which may have one or more substituent groups; W represents a carboxyl group; X represents a single bond, an oxygen atom, or a group represented by the various substituent groups including -NRX1CQ1O- (wherein Q1 represents an oxygen atom or a sulfur atom; RX1 represents a hydrogen atom, a cyano group, a formyl group, or various groups including a C1 to C6 alkyl group and a C1 to C6 hydroxyalkyl group, each of which may have one or more substituent groups) , ONRX1CQ1-, -NRX1CQ1-, -CQ1NRX1-, -NRX1aCQ1NRX1b-, -Q2SO2- and -SO2Q2-; Y represents a 5 to 14-membered aromatic group which may have one or more substituent groups and one or more hetero atoms, or a C3 to C7 alicyclic hydrocarbon group; and the rings Z and U may be the same as or different from each other and each represents a 5 to 14-membered aromatic group which may have 1 to 4 substituent groups and one or more hetero atoms, and the ring may be partially saturated.), a salt thereof, an ester thereof or a hydrate of them.

THE PYRIDYL CATION AS A REACTIVE INTERMEDIATE IN THE PHOTOREACTION OF IODOPYRIDINES WITH BENZENES

The electrophilic behavior of the reactive entity in the photosubstitution of benzenes with 2-iodopyridine was found to be ascribable to the intermediary 2-pyridyl cation, rather than the electrophilic 2-pyridyl radical.