74447-73-7

Basic information

• Product Name: 2-bromo-1-methoxy-4-phenyl-benzene
• Synonyms: 2-bromo-1-methoxy-4-phenyl-benzene
• CAS NO: 74447-73-7
• Molecular Formula: C₁₃H₁₁BrO
• Molecular Weight: 263.13
• Mol File: 74447-73-7.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 333.8°C at 760 mmHg
• Flash Point: 137.7°C
• Appearance: /
• Density: 1.35g/cm³
• Vapor Pressure: 0.000259mmHg at 25°C
• Refractive Index: 1.583
• CAS DataBase Reference: 2-bromo-1-methoxy-4-phenyl-benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 2-bromo-1-methoxy-4-phenyl-benzene(74447-73-7)
• EPA Substance Registry System: 2-bromo-1-methoxy-4-phenyl-benzene(74447-73-7)

Safety Data

• Hazardous Substances Data: 74447-73-7(Hazardous Substances Data)

Usage

General Description

2-bromo-1-methoxy-4-phenyl-benzene is a synthetic organic compound characterized by a benzene, or aromatic, ring structure. It contains a bromine atom, a methoxy group, and a phenyl group attached to the benzene ring. The respective positions of these substituent groups on the ring, as indicated by the numerical prefixes, are important for the compound's reactivity and its interactions in various chemical reactions. The input of these functional groups can significantly alter the properties and behaviors of the original benzene compound, including factors like boiling/melting points, polarity, and reactivity with other substances. Generally, such chemicals may be used in a variety of industries including pharmaceuticals, agrochemicals, and material sciences, though specific uses can vary greatly. Further specifics about 2-bromo-1-methoxy-4-phenyl-benzene such as its physical and chemical properties, safety, or use would involve advanced testing and detailed analysis.

InChI:InChI=1/C13H11BrO/c1-15-13-8-7-11(9-12(13)14)10-5-3-2-4-6-10/h2-9H,1H3

Upstream product

• 613-37-6 4-methoxylbiphenyl 
• 92-03-5 2-bromo-4-phenylphenol 
• 77-78-1 dimethyl sulfate 
• 67-66-3 chloroform 
• 7726-95-6 bromine 
• 21702-84-1 2,4-dibromoanisole 
• 92-69-3 4-Phenylphenol 
• 768-32-1 trimethylphenylsilane 
• 578-57-4 2-bromoanisole 
• 6943-73-3 N-(3-bromo-4-methoxyphenyl)acetamide 

Downstream Products

• 38088-00-5 4-methoxy-[1,1'-biphenyl]-2-amine 
• 102023-53-0 3-Brom-4-methoxy-4'-benzoyl-biphenyl 
• 102468-82-6 3-Brom-4-methoxy-4'-(4-methoxy-benzoyl)-biphenyl 
• 102468-80-4 3-Brom-4-methoxy-4'-phenacetyl-biphenyl 
• 102950-81-2 3-Brom-4-methoxy-4'-<4-tert.-butyl-benzoyl>-biphenyl 
• 670246-90-9 methanone, diphenyl-(4-methoxy-{1,1'-biphenyl}-3-yl)hydrazone 

Relevant articles and documents

A deacetylation-diazotation-coupling sequence: Palladium-catalyzed C-C bond formation with acetanilides as formal leaving groups

Acetanilides can be deacetylated and diazotized in situ, and subsequently used in Pd-catalyzed coupling reactions without isolation of the diazonium intermediate. Heck reactions, Suzuki crosscoupling reactions, and a Pd-catalyzed [2+2+1] cycloaddition hav

Solid-supported cross-coupling catalysts derived from homogeneous nickel and palladium coordination complexes

Solid-supported catalysts derived from homogeneous nickel(II) and palladium(II) non-symmetrical salen-type coordination complexes have been prepared and shown to be effective in the heterogeneous catalysis of carbon-carbon cross-coupling reactions. The nickel catalyst has been used in room-temperature Tamao-Kumada-Corriu reactions and the palladium catalyst in the Heck reaction at elevated temperatures. The complexes were prepared by improved methods and characterised by spectroscopic techniques. Comparisons between the solid-supported catalysts and their homogeneous analogues are reported. The single-crystal structure determination of the nickel and palladium complexes [M(salenac-OH)] [M= Ni, Pd; salenac-OH = 9-(2′,4′-dihydroxyphenyl)- 5,8-diaza-4-methylnona-2,4,8-trienato](2-)] is reported.