177976-31-7

Basic information

• Product Name: 3-(CHLOROMETHYL)-5-PHENYLPYRIDINE
• Synonyms: 3-(CHLOROMETHYL)-5-PHENYLPYRIDINE
• CAS NO: 177976-31-7
• Molecular Formula: C₁₂H₁₀ClN
• Molecular Weight: 203.67
• Mol File: 177976-31-7.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 343.002°C at 760 mmHg
• Flash Point: 191.913°C
• Appearance: /
• Density: 1.16g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.583
• CAS DataBase Reference: 3-(CHLOROMETHYL)-5-PHENYLPYRIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(CHLOROMETHYL)-5-PHENYLPYRIDINE(177976-31-7)
• EPA Substance Registry System: 3-(CHLOROMETHYL)-5-PHENYLPYRIDINE(177976-31-7)

Safety Data

• Hazardous Substances Data: 177976-31-7(Hazardous Substances Data)

Usage

General Description

3-(Chloromethyl)-5-phenylpyridine is a chemical compound that contains a pyridine ring with a phenyl and a chloromethyl group. It is mainly used as an intermediate in the synthesis of various pharmaceutical and agrochemical products. 3-(CHLOROMETHYL)-5-PHENYLPYRIDINE is known to have potential biological activity and has been studied for its anti-inflammatory and antibacterial properties. Additionally, 3-(chloromethyl)-5-phenylpyridine has been reported to have applications in the development of new materials and organic electronic devices due to its ability to form stable complexes with transition metal ions. However, it is important to note that this chemical should be handled with care as it can be hazardous if not used properly.

InChI:InChI=1/C12H10ClN/c13-7-10-6-12(9-14-8-10)11-4-2-1-3-5-11/h1-6,8-9H,7H2

Upstream product

• 187392-96-7 3-hydroxymethyl-5-phenyl-pyridine 

Downstream Products

• 280135-00-4 4-formyl-1-[(5-phenyl-3-pyridinyl)methyl]-indole 
• 177975-03-0 N-(5-phenyl-3-pyridylmethyl)-N-(2-chromanyl-methyl)-amine, maleate 

Relevant articles and documents

5-MEMBERED N-HETEROCYCLIC COMPOUNDS WITH HYPOGLYCEMIC AND HYPOLIPIDEMIC ACTIVITY

Use of a compound of the formula: wherein R represents a hydrocarbon group which may be substituted or a heterocyclic group which may be substituted; X represents a bond, an oxygen atom, a sulfur atom, or a group of the formula: -CO-, -CS-, -CR(OR)- or -NR- wherein each of R and R represents a hydrogen atom or a hydrocarbon group which may be substituted, R represents a hydrogen atom or a protective group for a hydroxyl group; m represents an integer of 0 to 3; Y represents an oxygen atom, a sulfur atom, or a group of the formula: -SO-, -SO2-, -NR-, -CONR- or -NRCO- wherein R represents a hydrogen atom or a hydrocarbon group which may be substituted; ring A represents an aromatic ring which may further have 1 to 3 substituents; n represents an integer of 1 to 8; ring B represents a nitrogen-containing 5-membered hetero ring which may further be substituted by an alkyl group; X represents a bond, an oxygen atom, a sulfur atom, or a group of the formula: -SO-, -SO2-, -O-SO2- or -NR- wherein R represents a hydrogen atom or a hydrocarbon group which may be substituted; R represents a hydrogen atom, a hydrocarbon group which may be substituted or a heterocyclic group which may be substituted; W represents a bond or a divalent hydrocarbon residue having 1 to 20 carbon atoms; R represents a group of the formula: -OR (R represents a hydrogen atom or a hydrocarbon group which may be substituted) or -NRR (each of R and R, whether identical or not, represents a hydrogen atom, a hydrocarbon group which may be substituted, a heterocyclic group which may be substituted, or an acyl group which may be substituted; R and R may bind together to form a ring); or a salt thereof, for the manufacture of a pharmaceutical preparation for preventing or treating syndrome X.