73709-54-3

Basic information

• Product Name: Cyclohexanone, 2-[(4-bromophenyl)hydroxymethyl]-
• CAS NO: 73709-54-3
• Molecular Formula: C13H15BrO2
• Molecular Weight: 283.165
• Mol File: 73709-54-3.mol
• Article Data: 108

Chemical Properties

• CAS DataBase Reference: Cyclohexanone, 2-[(4-bromophenyl)hydroxymethyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexanone, 2-[(4-bromophenyl)hydroxymethyl]-(73709-54-3)
• EPA Substance Registry System: Cyclohexanone, 2-[(4-bromophenyl)hydroxymethyl]-(73709-54-3)

Safety Data

• Hazardous Substances Data: 73709-54-3(Hazardous Substances Data)

Upstream product

• 108-94-1 cyclohexanone 
• 1122-91-4 4-bromo-benzaldehyde 
• 873-75-6 4-bromobenzenemethanol 
• 108-93-0 cyclohexanol 
• 1056477-06-5 2-bromocyclohexanone 
• 930-68-7 cyclohexenone 
• 37471-46-8 1-phenyl-1-trimethylsiloxypropene 
• 22780-11-6 1-(2,2,2-trichloroacetoxy)cyclohexene 
• 332041-60-8 Cyclohexanone trimethoxysilyl enol ether 
• 6651-36-1 1-(Trimethylsilyloxy)cyclohexene 

Downstream Products

• 586-76-5 4-Bromobenzoic acid 
• 108-93-0 cyclohexanol 
• 111729-78-3 (E)-2-(4-bromobenzylidene)cyclohexan-1-one 
• 111729-78-3 2-(4-Brom-benzyliden)cyclohexan-1-on 

Relevant articles and documents

Biomass waste-derived recyclable heterogeneous catalyst for aqueous aldol reaction and depolymerization of PET waste

In this work, we discuss the valorization of biomass waste-derived orange peel ash (OPA) by exploring its applicability as a heterogeneous catalyst in aqueous aldol reactions and demonstrating its versatility by promoting the methanolysis of poly(ethylene terephthalate) (PET) waste. The catalyst was characterized using Fourier-transform infrared spectroscopy (FT-IR), Brunauer-Emmett-Teller (BET) analysis, X-ray powder diffraction (XRD), X-ray fluorescence (XRF), energy dispersive X-ray (EDX) spectroscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and thermal gravimetric analysis (TGA) to decode its chemical composition. The aldol reactions were carried out at ambient temperature in the presence of water as a solvent. PET depolymerization was performed in an autoclave for 1 h using only 6% w/w OPA. The catalyst was recovered and reused in both the reactions for up to four successive cycles with minimal loss in the catalytic activity. The use of OPA as a cost-free, eco-friendly and effective recyclable catalyst enables a greener route for C-C bond formation and PET waste recycling.

Proline-Histidine Dipeptide: A Suitable Template for Generating Ion-Tagged Organocatalysts for the Asymmetric Aldol Reaction

Proline-histidine dipeptide laid the foundation for the construction of three new ion-tagged organocatalysts, utilising the imidazole moiety of histidine for generating the quaternary species. A brief comparative investigation of the catalysts in the enam

Pro-phe derivatives as organocatalysts in asymmetric aldol reaction

The aldol reaction which is the most important one among the C-C bond forming reactions, is widely used by synthetic organic chemists to obtain β-hydroxycarbonyl compounds which are important starting components for biologically active compounds in optica