167780-11-2

Basic information

• Product Name: 1-Propanone, 3-(2-chlorophenyl)-3-hydroxy-1-phenyl-
• CAS NO: 167780-11-2
• Molecular Formula: C15H13ClO2
• Molecular Weight: 260.72
• Mol File: 167780-11-2.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: 1-Propanone, 3-(2-chlorophenyl)-3-hydroxy-1-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Propanone, 3-(2-chlorophenyl)-3-hydroxy-1-phenyl-(167780-11-2)
• EPA Substance Registry System: 1-Propanone, 3-(2-chlorophenyl)-3-hydroxy-1-phenyl-(167780-11-2)

Safety Data

• Hazardous Substances Data: 167780-11-2(Hazardous Substances Data)

Usage

Physical state

White solid at room temperature

Common uses

Synthesis of pharmaceuticals, organic compounds, solvent, intermediate in chemical production

Industrial applications

Pharmaceutical and chemical industries

Ongoing research

Properties and potential uses

Upstream product

• 3300-67-2 3-(2-chlorophenyl)-1-phenylpropenone 
• 89-98-5 2-chloro-benzaldehyde 
• 98-86-2 acetophenone 
• 14762-47-1 2-diazo-3-oxo-3-phenylpropanal 
• 15397-33-8 3-Oxo-3-phenylpropanal 
• 65480-18-4 (3-(2-chlorophenyl)oxiran-2-yl)(phenyl)methanone 
• 70-11-1 α-bromoacetophenone 

Downstream Products

• 89-98-5 2-chloro-benzaldehyde 
• 98-86-2 acetophenone 

Relevant articles and documents

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A magnesium-based multifunctional metal-organic framework: Synthesis, thermally induced structural variation, selective gas adsorption, photoluminescence and heterogeneous catalytic study

Three magnesium based carboxylate framework systems were prepared through a temperature-dependent synthesis. The compounds were synthesized by a hydrothermal method and characterized by single crystal X-ray diffraction analysis. A stepwise increase in the

Biomimetic hydrogenation: A reusable NADH co-enzyme model for hydrogenation of α,β-epoxy ketones and 1,2-diketones

A biomimetic method has been developed to transform α,β-epoxy ketones or 1,2-diketones into corresponding β-hydroxy ketones or α-hydroxy ketones using a catalytic amount of BNAH or BNA +Br-. The regeneration of BNAH or BNA+Br - is achieved by a mixture of HCOOH/Et3N. A radical mechanism is proposed to explain these observations.