3382-65-8

Basic information

• Product Name: Phenol, 4-[[(4-bromophenyl)imino]methyl]-
• Synonyms: N-(4-Oxy-benzal)-4-brom-anilin;4-Hydroxy-benzaldehyd-semicarbazon;4-[(4-Brom-phenylimino)-methyl]-phenol;p-hydroxybenzaldehyde semicarbazone ester;p-Hydroxybenzaldehyde semicarbazone;4-[(4-bromo-phenylimino)-methyl]-phenol;N-(4-Oxy-benzyliden)-4-brom-anilin;4-hydroxy-benzaldehyde semicarbazone;p-Hydroxybenzaldehyd-Semicarbazon;4-Oxy-benzaldehyd-(4-brom-anil);4-hydroxybenzal semicarbazone;4-hydroxybenzal-4-bromoaniline;4-hydroxybenzylidene-4'-bromoaniline
• CAS NO: 3382-65-8
• Molecular Formula: C13H10BrNO
• Molecular Weight: 276.132
• Mol File: 3382-65-8.mol
• Article Data: 17

Chemical Properties

• CAS DataBase Reference: Phenol, 4-[[(4-bromophenyl)imino]methyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Phenol, 4-[[(4-bromophenyl)imino]methyl]-(3382-65-8)
• EPA Substance Registry System: Phenol, 4-[[(4-bromophenyl)imino]methyl]-(3382-65-8)

Safety Data

• Hazardous Substances Data: 3382-65-8(Hazardous Substances Data)

Upstream product

• 123-08-0 4-hydroxy-benzaldehyde 
• 106-40-1 4-bromo-aniline 
• 586-78-7 para-nitrophenyl bromide 
• 623-05-2 (4-hydroxyphenyl)methanol 
• 861556-73-2 4-[1-(4-bromo-phenyl)-3,4-diphenyl-[1,3]diazetidin-2-yl]-phenol 
• 64-17-5 ethanol 

Downstream Products

• 1095704-54-3 4-{4-[(4-bromo-phenylimino)-methyl]-phenoxymethyl}-7-methyl-chromen-2-one 
• 1095704-50-9 4-{4-[(4-bromo-phenylimino)-methyl]-phenoxymethyl}-6-methyl-chromen-2-one 
• 1393822-09-7 C₆₃H₆₆Br₃N₃O₆ 
• 1631129-33-3 C₅₇H₅₄Br₃N₃O₆ 
• 1631129-32-2 C₅₄H₄₈Br₃N₃O₆ 
• 1631129-20-8 C₁₆H₁₅Br₂NO 
• 16979-19-4 p-Acetoxybenzyliden-p-bromoanilin 
• 1354652-03-1 C₃₁H₄₄BrNO₂ 
• 1354652-02-0 C₂₉H₄₀BrNO₂ 
• 1354652-01-9 C₂₇H₃₆BrNO₂ 
• 1354651-99-2 C₂₃H₂₈BrNO₂ 
• 1354651-98-1 C₂₁H₂₄BrNO₂ 
• 1354652-00-8 C₂₅H₃₂BrNO₂ 
• 1266570-71-1 3-(4-bromophenyl)-2-(4-hydroxyphenyl)-5-methylthiazolidin-4-one 

Relevant articles and documents

Synthesis, identification, biological activity and anti-cancer activity Studies of Hetrocyclic Ligand Azo-schiff Base with Au(III) Complex

This research involved preparation of 2-((E)-(1H-benzo.[d]imidazol-2-yl).diazenyl)-4-(((4-bromophenyl)imino)methyl)phenol and Au(III) complex which was prepared by mixing solution of metal salt with ligand solution at mole ratio[ M:L] 1:1 . Compounds prep

Simple synthesis of the novel Cu-MOF catalysts for the selective alcohol oxidation and the oxidative cross-coupling of amines and alcohols

A novel porous metal–organic framework {Cu2(bbda)0.5(Hbbda)1.5(OAc)1.5.8H2O} (UoB-5) was synthesized under ultrasound irradiation by employing a new Schiff base ligand H2bbda (4,4'(1,4-phenylene bis (azanylylidene)) bis (methanylylidene))dibenzoic acid) and was fully characterized. The microporous nature of UoB-5 was confirmed by gas-sorption measurements. This framework acted as a highly effective heterogeneous catalyst for the alcohol oxidation reaction with tert-butyl hydroperoxide (t-BuOOH) as an oxidant. The presence of coordinatively unsaturated metal sites in UoB-5 could be the reason for high performance in this reaction. Furthermore, using the long linker with the free -NC group and uncoordinated -N atom on the wall of the pores created UoB-5 an excellent candidate for the catalytic activities without activation of the framework. It was confirmed with the heterogeneous catalytic experiments on the one-pot tandem synthesis of imines from benzyl alcohols and anilines. Eventually, the new Cu-MOF (UoB-5) could be an alternative catalyst as a more economically favorable and environmentally friendly in the catalysis field.

Effect of substituents on the UV spectra of supermolecular system: Silver nanoparticles with bi-aryl Schiff bases containing hydroxyl

Effect of substituents on the ultraviolet (UV) spectra of supermolecular system involving silver nanoparticles (AgNPs) and Schiff bases was investigated. AgNPs and 49 samples of model compounds (MC), bi-aryl Schiff bases containing hydroxyl (XBAY, involving 4-OHArCH?NArY, 2-OHArCH?NArY, XArCH?NAr-4′-OH, and XArCH?NAr-2′-OH), were synthesized. The size of AgNPs was characterized by transmission electron microscopy (TEM), and the UV absorption spectra of AgNPs, XBAYs, and MC-AgNPs mixed solutions were measured, respectively. The results show that (1) the size of AgNPs is larger in MC-AgNPs solutions than that in AgNPs solution due to the distribution of MC molecules on the surface of AgNPs; (2) the UV absorption wavelength of XBAYs changes in the action of AgNPs and their wavelength shift exists limitation between XBAY and MC-AgNPs solutions; and (3) the wavelength shift limit of MC-AgNPs (λWSL) is influenced by the substituents X and Y and the position of hydroxyl OH. The wavenumber ΔνWSL of λWSL can be quantified by employing the excited-state substituent constant σexCC and Hammett constant σ of substituents X and Y. Comparing with the 4-OH, the 4′-OH makes the ΔνWSL a red shift, whereas the 2′-OH, comparing with the 2-OH, makes the ΔνWSL a blue shift.