256372-73-3

Basic information

• Product Name: Oxirane, [(2,3-dimethylphenoxy)methyl]-, (2S)-
• CAS NO: 256372-73-3
• Molecular Formula: C11H14O2
• Molecular Weight: 178.231
• Mol File: 256372-73-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Oxirane, [(2,3-dimethylphenoxy)methyl]-, (2S)-(CAS DataBase Reference)
• NIST Chemistry Reference: Oxirane, [(2,3-dimethylphenoxy)methyl]-, (2S)-(256372-73-3)
• EPA Substance Registry System: Oxirane, [(2,3-dimethylphenoxy)methyl]-, (2S)-(256372-73-3)

Safety Data

• Hazardous Substances Data: 256372-73-3(Hazardous Substances Data)

Upstream product

• 41457-31-2 1,2-epoxy-3-[2,3-dimethylphenoxy]propane 
• 526-75-0 2,3-Dimethylphenol 
• 850427-86-0 (2S)-1-(2,3-dimethylphenoxy)-2,3-dihydroxypropane 
• 3731-94-0 allyl 2,3-dimethylphenyl ether 
• 850427-90-6 (R)-4-(2,3-Dimethyl-phenoxymethyl)-[1,3,2]dioxathiolane 2-oxide 
• 850427-96-2 (R)-4-(2,3-Dimethyl-phenoxymethyl)-[1,3,2]dioxathiolane 2,2-dioxide 

Downstream Products

• 81584-06-7 1-(tert-butylamino)-3-(2,3-dimethylphenoxy)-2-propanol 

Relevant articles and documents

Synthesis, crystal structure, and absolute configuration of the enantiomers of chiral drug xibenolol hydrochloride

Based on the features of its crystallization, racemic 3-(2,3-dimethylphenoxy)propane-1,2-diol 2, the synthetic precursor of the chiral drug xibenolol 1, was resolved into pure enantiomers by the direct method of entrainment. The enantiomers of diol 2 thro

Asymmetric synthesis of aryloxypropanolamines via OsO4-catalyzed asymmetric dihydroxylation

A simple and effective procedure for the enantioselective synthesis of several β-adrenergic blocking agents incorporating the first asymmetric synthesis of celiprolol, is described. The key steps are (i) sharpless asymmetric dihydroxylation of aryl allyl ethers to introduce chirality into the molecules and (ii) conversion of cyclic sulfates into the corresponding epoxides using a three-step procedure.