3164-13-4

Basic information

• Product Name: 2-(4-BROMO-PHENYL)-BENZOOXAZOLE
• Synonyms: CHEMBRDG-BB 4010236;2-(4-BROMO-PHENYL)-BENZOOXAZOLE;2-(4-bromophenyl)-1,3-benzoxazole(SALTDATA: FREE);2-(4-Bromophenyl)-1,3-benzoxazole;2-(p-Bromophenyl)benzoxazole;Benzoxazole,2-(4-bromophenyl)-
• CAS NO: 3164-13-4
• Molecular Formula: C₁₃H₈BrNO
• Molecular Weight: 274.11272
• Mol File: 3164-13-4.mol
• Article Data: 123

Chemical Properties

• Melting Point: 158-159℃
• Boiling Point: 339℃
• Flash Point: 159℃
• Appearance: /
• Density: 1.514
• Vapor Pressure: 0.000185mmHg at 25°C
• Refractive Index: 1.659
• Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
• Solubility: soluble in Toluene
• PKA: 0.88±0.10(Predicted)
• CAS DataBase Reference: 2-(4-BROMO-PHENYL)-BENZOOXAZOLE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-BROMO-PHENYL)-BENZOOXAZOLE(3164-13-4)
• EPA Substance Registry System: 2-(4-BROMO-PHENYL)-BENZOOXAZOLE(3164-13-4)

Safety Data

• Hazardous Substances Data: 3164-13-4(Hazardous Substances Data)

Usage

Physical Form

Solid

Uses

2-(4-Bromo-Phenyl)-Benzooxazole (cas# 3164-13-4) is a useful research chemical.

InChI:InChI=1/C13H8BrNO/c14-10-7-5-9(6-8-10)13-15-11-3-1-2-4-12(11)16-13/h1-8H

Upstream product

• 1122-91-4 4-bromo-benzaldehyde 
• 95-55-6 2-amino-phenol 
• 698-67-9 p-bromobenzamide 
• 117649-27-1 2-(4-bromo-benzylidenamino)-phenol 
• 349613-49-6 4-bromo-N-(2-bromophenyl)benzamide 
• 615-36-1 2-bromoaniline 
• 95-51-2 o-chloroaniline 
• 586-75-4 4-chlorobenzoyl chloride 
• 6192-52-5 p-toluenesulfonic acid monohydrate 
• 346689-26-7 N-(2-iodophenyl)-4-bromobenzamide 
• 313268-56-3 C₁₃H₉BrClNO 
• 1268386-95-3 C₁₃H₁₀BrNO 
• 273-53-0 benzoxazole 
• 41018-52-4 (4-bromophenyl)-λ³-iodanediyl diacetate 

Downstream Products

• 833-50-1 2-phenylbenzo[d]oxazole 
• 439090-73-0 (2-(benzo[d]oxazol-2-yl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 1159445-47-2 4-(benzoxazol-2-yl)-4'-(3-phenylquinoxalin-2-yl)triphenylamine 
• 1196685-64-9 2,2'-[2,2'-bipyridine-5,6-diylbis(biphenyl-4,4'-diyl)]bisbenzoxazole 
• 1196685-66-1 2,2'-[2,3'-bipyridine-5,6-diylbis(biphenyl-4,4'-diyl)]bisbenzoxazole 
• 1196685-69-4 2,2'-[2,4'-bipyridine-5,6-diylbis(biphenyl-4,4'-diyl)]bisbenzoxazole 
• 1196685-73-0 2,2'-[2-(bipyridin-2-yl)pyridine-5,6-diylbis(biphenyl-4,4'-diyl)]bisbenzoxazole 

Relevant articles and documents

Tertiary amine derivatives and organic electroluminescent device including the same

A UV-region high-energy external light source is effectively absorbed to minimize damage to organic materials in the organic electroluminescent device. 1 Is a cross-sectional view of an organic electroluminescence device according to the present invention. O-2 electrode 1 Or more organic material layers disposed between the (2) and (1) th electrodes. A capping layer is included. The organic material layer and/or the capping layer may include the 1 st amine derivative represented by Formula 3. Chemical Formula 1. Wherein each substituent in Formula 1 is as defined in the description of the invention.

An efficient rapid synthesis of benzoxazoles and benzothiazoles using pma.Sio2 at room temperature under heterogeneous conditions

Treatment of 2-aminophenol (or 2-aminothiophenol) with aromatic aldehydes in the presence of phosphomolybdic acid on silica at room temperature affords the corresponding benzoxazoles (or benzothiazoles) in excellent yields (88-96%) under heterogeneous conditions. Benzoxazoles and benzothiazoles are formed in less than 10 min.

Heterogeneous palladium (II)-complexed dendronized polymer: A rare palladium catalyst for the one-pot synthesis of 2-arylbenzoxazoles

The palladium complex of dendronized amine polymer (EG–Gn–Pd, n = 0, 1 and 2) having ethylene glycol-initiated polyepichlorohydrin as core was synthesized on a Merrifield resin support and was well characterized. Generally, palladium catalysts are known for carbon–carbon coupling reactions. Here, a developed catalyst was found to be good for benzoxazole synthesis. Higher generation dendronized polymer (EG–G2–Pd) was found to be better catalyst over lower generation dendronized polymers. Moreover, dendronized polymers were found to be a better catalyst over dendrigraft polymers. The catalyst reusability was checked and good yield was obtained for five cycles.