16372-96-6

Basic information

• Product Name: 3,5-DibroMo-biphenyl
• Synonyms: 3,5-DibroMo-biphenyl;3,5-DIBROMO-1-PHENYLBENZENE;PBB 14
• CAS NO: 16372-96-6
• Molecular Formula: C₁₂H₈Br₂
• Molecular Weight: 311.99992
• Mol File: 16372-96-6.mol
• Article Data: 22

Chemical Properties

• Melting Point: 156-157℃
• Boiling Point: 334.6°Cat760mmHg
• Flash Point: 181.3°C
• Appearance: /
• Density: 1.667g/cm³
• Vapor Pressure: 0.000246mmHg at 25°C
• Refractive Index: 1.6541 (589.3 nm 25℃)
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 3,5-DibroMo-biphenyl(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-DibroMo-biphenyl(16372-96-6)
• EPA Substance Registry System: 3,5-DibroMo-biphenyl(16372-96-6)

Safety Data

• Hazardous Substances Data: 16372-96-6(Hazardous Substances Data)

Usage

Chemical Properties

Colorless liquid

InChI:InChI=1/C12H8Br2/c13-11-6-10(7-12(14)8-11)9-4-2-1-3-5-9/h1-8H

Upstream product

• 16372-95-5 2.4-Dibrom-6-phenylanilin 
• 626-39-1 1,3,5-trisbromobenzene 
• 98-80-6 phenylboronic acid 
• 71-43-2 benzene 
• 19752-57-9 1,3-dibromo-5-iodobenzene 
• 92-67-1 4-phenylalanine 
• 855256-46-1 3,5-dibromo-4'-nitro-1,1'-biphenyl 
• 860572-11-8 N-biphenyl-2-yl-N-chloro-acetamide 
• 3477-62-1 2,4'-Diamino-4-nitro-biphenyl 
• 7147-52-6 N-(5-bromo-[1,1'-biphenyl]-2-yl)acetamide 
• 2113-47-5 2-acetamidobiphenyl 
• 86-00-0 2-nitrobiphenyl 
• 854662-21-8 4-amino-3',5'-dibromobiphenyl 
• 3366-59-4 4-amino-3,5-dibromo-1,1'-biphenyl 

Downstream Products

• 4445-59-4 [1,1'-biphenyl]-3,5-dicarboxylic acid 
• 92-52-4 biphenyl 
• 2113-57-7 3-bromobiphenyl 
• 580-51-8 [1,1'-biphenyl]-3-ol 
• 108-95-2 phenol 
• 1189047-30-0 C₄₈H₃₂N₂ 

Relevant articles and documents

CuI in biorenewable basic medium: Three novel and low E-factor Suzuki-Miyaura cross-coupling reactions

In this article, we have disclosed three inexpensive and novel copper-catalyzed C(sp2)–C(sp2) coupling reactions of substituted aryl/heteroaryl halides with arylboronic acids by employing water extract of pomegranate ash (WEPA) as biorenewable base and aqueous reaction medium. CuI/WEPA, CuI/WEPA/DABCO, CuI/WEPA/SPhos catalytic systems were developed for the present Suzuki-Miyaura coupling. WEPA has been found to be the effective base and reaction medium for copper-catalysed Suzuki-Miyaura reactions with and without ligands to provide good to high yields of coupling products. This method has remarkable advantages like inexpensive and waste-derived biorenewable base, low catalyst loading, moderate temperature, replacement of precious palladium with abundant copper, no or negligible contamination of copper in products, low E-factor, high chemoselectivity and a large substrate scope.

Organic compound, and organic electroluminescent device and electronic device using same

The invention relates to an organic compound. The structure of the organic compound comprises a formula I. When the organic compound provided by the invention is used for a light-emitting layer of anorganic electroluminescent device, the device efficiency of the device can be effectively improved, and the service life of the organic electroluminescent device is prolonged.

Phosphorescent OLED and hole transporting materials for phosphorescent OLEDS

The present invention relates to phosphorescent organic light-emitting diodes (OLEDs) including a hole-transporting or a hole-transporting and an electron-blocking layer including an N,N,N′,N′-tetraaryl-phenylene-3,5-diamine or an N,N,N′,N′-tetraaryl-1,1′-biphenyl-3,3′-diamine matrix compound and to new N,N,N′,N′-tetraarylsubstituted m-arylene diamine compounds useful as hole-transporting and electron-blocking layer matrices in phosphorescent OLEDs.