51339-30-1

Basic information

• Product Name: BenzeneMethanol, 3-broMo-alpha-(3-broMophenyl)-
• Synonyms: BenzeneMethanol, 3-broMo-alpha-(3-broMophenyl)-;Bis(3-broMophenyl)Methanol
• CAS NO: 51339-30-1
• Molecular Formula: C₁₃H₁₀Br₂O
• Molecular Weight: 342.0259
• Mol File: 51339-30-1.mol
• Article Data: 9

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: BenzeneMethanol, 3-broMo-alpha-(3-broMophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: BenzeneMethanol, 3-broMo-alpha-(3-broMophenyl)-(51339-30-1)
• EPA Substance Registry System: BenzeneMethanol, 3-broMo-alpha-(3-broMophenyl)-(51339-30-1)

Safety Data

• Hazardous Substances Data: 51339-30-1(Hazardous Substances Data)

Upstream product

• 3132-99-8 m-bromobenzoic aldehyde 
• 591-18-4 1-Bromo-3-iodobenzene 
• 108-36-1 1,3-dibromobenzene 
• 2592-86-1 (m-Bromophenyl)lithium 
• 25032-74-0 3,3'-dibromobenzophenone 

Downstream Products

• 1569852-62-5 C₃₈H₄₂B₂O₄ 
• 1569852-68-1 C₆₂H₄₆N₂ 
• 1569852-74-9 C₆₂H₄₆N₂ 
• 1569852-71-6 C₆₂H₄₆N₂ 
• 25032-74-0 3,3'-dibromobenzophenone 
• 51339-16-3 3,3'-Dibrom-benzhydrylbromid 

Relevant articles and documents

Fused ring compound as well as preparation method and application thereof as well as CO-host material Light-emitting composition, light-emitting device, lighting apparatus, and display apparatus

Disclosed are fused ring compounds having a structure represented by Formula 1 or Formula 2, a method for preparing the same, a co-host material containing the condensed cyclic compound, a light emitting composition, a light emitting device and containing

Substituted carbazole diphenyl ketone compound and an organic electroluminescence element

PROBLEM TO BE SOLVED: To provide a novel compound which is a low-molecular material having both of sufficiently high excitation triplet energy and a charge injection-transport property, which is scarcely soluble in an alcoholic solvent, and with which a f

Construction of efficient blue AIE emitters with triphenylamine and TPE moieties for non-doped OLEDs

In this paper, by merging the hole-dominated triphenylamine (TPA) and tetraphenylethene (TPE) moieties together with different linkage positions, four derivatives of 1,2-bis[4′-(diphenylamino)biphenyl-4-yl]-1,2- diphenylethene (2TPATPE) were successfully synthesized with confirmed structures, and their thermal, optical and electronic properties were fully investigated. Thanks to the introduction of the meta-linkage mode on the TPE core, their π-conjugation length could be effectively restricted to ensure blue emission. The non-doped OLEDs based on these four emitters exhibit blue emissions from 443-466 nm, largely blue-shifted with respect to the green emission of 2TPATPE (514 nm). Meanwhile, good electroluminescence efficiencies with Lmax, ηC,max, and ηP,max of up to 8160 cd m-2, 3.79 cd A-1, and 2.94 Im W-1 respectively, have also been obtained, further validating our rational design of blue AIE fluorophores. The Royal Society of Chemistry.