1249756-52-2

Basic information

• Product Name: [1‐(4‐bromo‐phenyl)‐1H‐[1,2,3]triazol‐4‐yl]‐methanol
• Synonyms: [1‐(4‐bromo‐phenyl)‐1H‐[1,2,3]triazol‐4‐yl]‐methanol
• CAS NO: 1249756-52-2
• Molecular Weight: 254.086
• Mol File: 1249756-52-2.mol
• Article Data: 19

Chemical Properties

• CAS DataBase Reference: [1‐(4‐bromo‐phenyl)‐1H‐[1,2,3]triazol‐4‐yl]‐methanol(CAS DataBase Reference)
• NIST Chemistry Reference: [1‐(4‐bromo‐phenyl)‐1H‐[1,2,3]triazol‐4‐yl]‐methanol(1249756-52-2)
• EPA Substance Registry System: [1‐(4‐bromo‐phenyl)‐1H‐[1,2,3]triazol‐4‐yl]‐methanol(1249756-52-2)

Safety Data

• Hazardous Substances Data: 1249756-52-2(Hazardous Substances Data)

Upstream product

• 107047-10-9 p-bromobenzylazide 
• 107-19-7 propargyl alcohol 
• 106-40-1 4-bromo-aniline 
• 2101-88-4 1-azido-4-bromobenzene 

Downstream Products

• 1325725-16-3 1-(4-bromophenyl)-4-(fluoromethyl)-1H-1,2,3-triazole 
• 1373934-11-2 1-{3-[(1-(4-bromophenyl)-1H-[1,2,3]triazol-4-yl)methoxy]-2-hydroxypropyl}-2-hydroxymethyl-piperidine-3,4,5-triol 
• 1373934-06-5 C₁₂H₁₂BrN₃O₂ 
• 944901-52-4 1-(4-bromophenyl)-1H-1,2,3-triazol-4-yl carboxylic acid 
• 20320-17-6 1-(4-bromophenyl)-1H-1,2,3-triazole 
• 916151-04-7 1-(4-bromophenyl)-1H-1,2,3-triazole-4-carbaldehyde 

Relevant articles and documents

(DHQD)2PHAL ligand-accelerated Cu-catalyzed azide-alkyne cycloaddition reactions in water at room temperature

Herein, we have described, a 'Click Chemistry' protocol for the rapid synthesis of 1,2,3-triazoles in water. (DHQD)2PHAL has been found to be an excellent accelerating ligand for the copper(i)-catalyzed azide-alkyne cycloaddition reaction under

Anti-Lung Cancer Activities of 1,2,3-Triazole Curcumin Derivatives via Regulation of the MAPK/NF-κB/STAT3 Signaling Pathways

In this study, a series of curcumin derivatives containing 1,2,3-triazole were designed and synthesized, and their inhibitory activities against the proliferation of lung cancer cells were studied. Compound 5 k (3,4-dichlorobenzyltriazole methyl curcumin)

Alternative Route Triggering Multistep Spin Crossover with Hysteresis in an Iron(II) Family Mediated by Flexible Anion Ordering

Multistep spin crossover (SCO) compounds have attracted much attention, since they can be great candidates for high-density multinary memory devices. The introduction of substituents, such as methyl (Me), chloro (Cl), bromo (Br), and methoxy (MeO) groups,

Cu nanoparticles immobilized on modified magnetic zeolite for the synthesis of 1,2,3-triazoles under ultrasonic conditions

Magnetically recoverable copper nanoparticle-loaded natural zeolite (CuNPs/MZN) as an efficient catalyst was synthesized. The Fe3O4 magnetic nanoparticles were immobilized into the pores of natural clinoptilolite zeolite, which were