22464-01-3

Basic information

• Product Name: erythro-2-hydroxy-3-chloro-1,3-diphenyl-1-propanone
• CAS NO: 22464-01-3
• Molecular Weight: 260.72
• Mol File: 22464-01-3.mol

Chemical Properties

• CAS DataBase Reference: erythro-2-hydroxy-3-chloro-1,3-diphenyl-1-propanone(CAS DataBase Reference)
• NIST Chemistry Reference: erythro-2-hydroxy-3-chloro-1,3-diphenyl-1-propanone(22464-01-3)
• EPA Substance Registry System: erythro-2-hydroxy-3-chloro-1,3-diphenyl-1-propanone(22464-01-3)

Safety Data

• Hazardous Substances Data: 22464-01-3(Hazardous Substances Data)

Upstream product

• 7570-85-6 trans-2,3-epoxy-1,3-diphenyl-1-propanone 
• 5411-12-1 chalcone epoxide 
• 7646-78-8 tin(IV) chloride 
• 71-43-2 benzene 
• 7647-01-0 hydrogenchloride 
• 60-29-7 diethyl ether 

Downstream Products

• 7570-85-6 trans-2,3-epoxy-1,3-diphenyl-1-propanone 
• 5411-12-1 (2S,3R)-phenyl(3-phenyloxiran-2-yl)methanone 
• 5411-12-1 trans-(2S,3R)-epoxy-1,3-diphenylpropan-1-one 

Relevant articles and documents

Synthesis of β-chlorohydrins in water

2,4,6-Trichloro-1,3,5-triazine (TCT, cyanuric chloride) was found to mediate the regio- and stereoselective ring opening of epoxides in H 2O in the presence of morpholine at room temperature to afford the corresponding β-chlorohydrins in excellent yields (Table). The transformation is very simple, fast, efficient, and ecologically beneficial.

Regio- and stereoselective reaction of α-epoxyketones with AlCl 3: An efficient approach for the synthesis of functionalized β-chlorohydrines

A simple and efficient synthesis of functionalized β-chlorohydrins is described from the regio- and stereoselective reaction of α-epoxyketones with AlCl3 in acetonitrile at room temperature.

DICHLORODIISOPROPOXYTITANIUM - A CONVENIENT REAGENT FOR THE SELECTIVE TRANSFORMATIONS OF α,β-EPOXYCARBONYL COMPOUNDS

Depending on the structure and the reaction conditions, α,β-epoxycarbonyl compounds isomerize selectively in the presence of dichlorodiisopropoxytitanium to α-diketones or undergo nucleophilic cleavage with the formation of the corresponding hydroxychloro ketones.

An Easy and Efficient Epoxide Opening to give Halohydrins using Tin(II) Halides

Epoxides are readily converted into halohydrins by tin(II) halides in a variety of solvents.

Substituent Effects in 13C-N.M.R. Spectra of Diastereomeric Chalcone Dihalogenides. V. Synthesis, Stereochemistry and Spectroscopy of Chalcone Fluorohydrines

Chalcone fluorohydrins 1 and diastereomeric pairs of chalcone chlorohydrins 2 as standards are investigated in the i.r., 1H, 19F, and 13C n.m.r. spectroscopy field.The substituent dependence of the spectral parameters is discussed.The assignment of confor

The Behaviour of Functionally Epoxycarbonyl Compounds with the Reaction of Hydrogen Chloride

The Conversion of the Mannich base 2 to the hydrochloride proceeds with opening of the oxirane ring yielding 4*2HCl.Contrary to the results with formerly examined epoxides of the chalcone type here in polar as in apolar medium the formation of the erythro