18951-46-7

Basic information

• Product Name: 4-[(E)-2-(4-chlorophenyl)ethenyl]phenol
• Synonyms: 4-Chloro-4'-hydroxy-E-stilbene; Phenol, 4-[(E)-2-(4-chlorophenyl)ethenyl]-
• CAS NO: 18951-46-7
• Molecular Formula: C₁₄H₁₁ClO
• Molecular Weight: 230.6895
• Mol File: 18951-46-7.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 372.1°C at 760 mmHg
• Flash Point: 178.8°C
• Density: 1.26g/cm³
• Vapor Pressure: 4.61E-06mmHg at 25°C
• Refractive Index: 1.695
• CAS DataBase Reference: 4-[(E)-2-(4-chlorophenyl)ethenyl]phenol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-[(E)-2-(4-chlorophenyl)ethenyl]phenol(18951-46-7)
• EPA Substance Registry System: 4-[(E)-2-(4-chlorophenyl)ethenyl]phenol(18951-46-7)

Safety Data

• Hazardous Substances Data: 18951-46-7(Hazardous Substances Data)

Upstream product

• 1878-66-6 4-chlorophenylacetic Acid 
• 123-08-0 4-hydroxy-benzaldehyde 
• 7400-08-0 p-Coumaric Acid 
• 106-47-8 4-chloro-aniline 
• 99-93-4 4-Hydroxyacetophenone 
• 74-11-3 para-chlorobenzoic acid 
• 7647-01-0 hydrogenchloride 
• 3926-62-3 sodium monochloroacetic acid 
• 67-64-1 acetone 
• 1073-67-2 4-vinylbenzyl chloride 
• 2628-17-3 4-Vinylphenol 
• 106-41-2 4-bromo-phenol 
• 540-38-5 p-Iodophenol 
• 637-87-6 1-Chloro-4-iodobenzene 

Downstream Products

• 131530-00-2 C₁₇H₁₆BrClO 
• 1588534-24-0 C₂₈H₂₀Cl₂O₂ 
• 20357-42-0 N-(4-chlorobenzyl)-4-methoxyaniline 
• 73351-21-0 4-(((4-methoxyphenyl)amino)methyl)phenol 
• 127066-88-0 2-(5-{4-[(E)-2-(4-Chloro-phenyl)-vinyl]-phenoxy}-pentylsulfanyl)-6-oxo-1,6-dihydro-pyrimidine-4-carboxylic acid 
• 127066-87-9 2-(3-{4-[(E)-2-(4-Chloro-phenyl)-vinyl]-phenoxy}-propylsulfanyl)-6-oxo-1,6-dihydro-pyrimidine-4-carboxylic acid 
• 127066-95-9 2-(5-{4-[(E)-2-(4-Chloro-phenyl)-vinyl]-phenoxy}-pentylsulfanyl)-6-methyl-3H-pyrimidin-4-one 
• 127066-94-8 2-(3-{4-[(E)-2-(4-Chloro-phenyl)-vinyl]-phenoxy}-propylsulfanyl)-6-methyl-3H-pyrimidin-4-one 
• 127066-84-6 2-(5-{4-[(E)-2-(4-Chloro-phenyl)-vinyl]-phenoxy}-pentylsulfanyl)-3H-pyrimidin-4-one 
• 127066-83-5 2-(3-{4-[(E)-2-(4-Chloro-phenyl)-vinyl]-phenoxy}-propylsulfanyl)-3H-pyrimidin-4-one 
• 118481-65-5 2-{4-[(E)-2-(4-Chloro-phenyl)-vinyl]-phenoxy}-propionic acid hydrazide 
• 118481-59-7 2-{4-[(E)-2-(4-Chloro-phenyl)-vinyl]-phenoxy}-propionic acid 
• 118481-64-4 {4-[(E)-2-(4-Chloro-phenyl)-vinyl]-phenoxy}-acetic acid hydrazide 
• 118481-58-6 E-4'-chloro-4-carboxymethoxystilbene 

Relevant articles and documents

Synthesis and biological evaluation of halogenated e-stilbenols as promising antiaging agents

The increased risk of illness and disability is related to the age inevitable biological changes. Oxidative stress is a proposed mechanism for many age-related diseases. The crucial importance of polyphenol pharmacophore for aging process is largely descr

Iron-Catalyzed Nitrene Transfer Reaction of 4-Hydroxystilbenes with Aryl Azides: Synthesis of Imines via C=C Bond Cleavage

C=C bond breaking to access the C=N bond remains an underdeveloped area. A new protocol for C=C bond cleavage of alkenes under nonoxidative conditions to produce imines via an iron-catalyzed nitrene transfer reaction of 4-hydroxystilbenes with aryl azides is reported. The success of various sequential one-pot reactions reveals that the good compatibility of this method makes it very attractive for synthetic applications. On the basis of experimental observations, a plausible reaction mechanism is also proposed.

Aerobic oxidative coupling of resveratrol and its analogues by visible light using mesoporous graphitic carbon nitride (mpg-C3N4) as a bioinspired catalyst

The first aerobic oxidative coupling of resveratrol and its analogues by mesoporous graphitic carbon nitride as a bioinspired catalyst with visible light has been developed. With this method, δ-viniferin and its analogues were synthesized in moderate to high yield. The metal-free conditions, visible-light irradiation, and the ideal oxidant, molecular oxygen, make this coupling reaction environmental friendly and practical. Copyright