2502-99-0

Basic information

• Product Name: 4-Chlorostilbazole
• Synonyms: 4-(4-Chlorostyryl)pyridine;4-Chlorostilbazole;(E)-4-(4-chlorostyryl)pyridine
• CAS NO: 2502-99-0
• Molecular Formula: C₁₃H₁₀ClN
• Molecular Weight: 215.6782
• Mol File: 2502-99-0.mol
• Article Data: 4

Chemical Properties

• Melting Point: 110 °C
• Boiling Point: 346.7°C at 760 mmHg
• Flash Point: 194.3°C
• Appearance: /
• Density: 1.212g/cm³
• Vapor Pressure: 0.000114mmHg at 25°C
• Refractive Index: 1.672
• PKA: 5.63±0.10(Predicted)
• CAS DataBase Reference: 4-Chlorostilbazole(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Chlorostilbazole(2502-99-0)
• EPA Substance Registry System: 4-Chlorostilbazole(2502-99-0)

Safety Data

• Hazardous Substances Data: 2502-99-0(Hazardous Substances Data)

Usage

InChI:InChI=1/C13H10ClN/c14-13-5-3-11(4-6-13)1-2-12-7-9-15-10-8-12/h1-10H

Upstream product

• 104-83-6 1-Chloro-4-(chloromethyl)benzene 
• 872-85-5 pyridine-4-carbaldehyde 
• 39225-17-7 diethyl 4-chlorobenzylphosphonate 
• 100-43-6 4-vinylpyridine 
• 1679-18-1 4-Chlorophenylboronic acid 

Downstream Products

• 2116-64-5 4-(2-phenylethyl)pyridine 
• 86590-58-1 1-(Adamant-1-yl)-1-phenyl-2-(pyrid-4-yl)-ethan 
• 86590-57-0 1-(Adamant-1-yl)-2-phenyl-1-(pyrid-4-yl)-ethan 
• 142937-28-8 4-(4-chloro-trans-styryl)-pyridine; hydrochloride 
• 73675-30-6 rac-4,4'-((1R,2R,3S,4S)-2,4-bis(4-chlorophenyl)cyclobutane-1,3-diyl)dipyridine 
• 85680-75-7 mer-(Ru(trpy)(4'-Cl-stilb)3)(PF₆)2 
• 85717-45-9 cis-(Ru(bpy)2(4'-Cl-stilb)2)(PF₆)2 
• 85717-51-7 (Ru(trpy)(bpy)(4'-Cl-stilb))(PF₆)2 
• 5847-63-2 cis-4'-Chlor-4-stilbazol 
• 25514-82-3 4-(4-chloro-trans-styryl)-1-methyl-pyridinium; iodide 

Relevant articles and documents

A new insight into the push-pull effect of substituents via the stilbene-like model compounds

In this paper, authors report on 1-pyridyl-2-arylethenes, 1-furyl-2-arylethylenes, 1,2-diphenylpropylenes and substituted cinnamyl anilines as stilbene-like model compounds to investigate the factors dominating the push-pull effect of substituents via usi

Ligand-free palladium-catalysed oxidative Heck reaction of 4-vinylpyridine with arylboronic acids: Selective synthesis of (E)-4-styrylpyridines

A ligand-free palladium-catalysed oxidative Heck reaction of various arylboronic acids with 4-vinylpyridine has been developed, achieving (E)-4-styrylpyridines with high selectively in moderate to good yields. A plausible mechanism for the formation of (E)-4-styrylpyridines has been proposed.