32345-63-4

Basic information

• Product Name: 1-(3-methoxyphenyl)-1,2-ethanediol
• CAS NO: 32345-63-4
• Molecular Weight: 168.192
• Mol File: 32345-63-4.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 1-(3-methoxyphenyl)-1,2-ethanediol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(3-methoxyphenyl)-1,2-ethanediol(32345-63-4)
• EPA Substance Registry System: 1-(3-methoxyphenyl)-1,2-ethanediol(32345-63-4)

Safety Data

• Hazardous Substances Data: 32345-63-4(Hazardous Substances Data)

Upstream product

• 5000-65-7 2-bromo-3'-methoxyacetophenone 
• 586-37-8 1-(3-Methoxyphenyl)ethanone 
• 2398-37-0 3-methoxyphenyl bromide 
• 83585-22-2 methyl 2-(3-methoxyphenyl)-2-oxoacetate 
• 626-20-0 3-methoxystyrene 
• 32025-65-3 3-methoxyphenylglyoxal 
• 6814-64-8 methylenedimethyl sulfurane 
• 591-31-1 3-methoxy-benzaldehyde 
• 108379-93-7 α-acetoxy-3-methoxyacetophenone 

Downstream Products

• 136178-90-0 1-ethoxyethyl 2-methoxy-2-(3-methoxyphenyl)ethyl ether 
• 71897-08-0 2-(3-methoxyphenyl)quinoxaline 
• 136179-06-1 1-methoxy-1-(3-methoxyphenyl)ethylene 
• 329346-52-3 (S)-1-(m-methoxy phenyl)ethane-1,2-diol 
• 41252-80-6 2-chloro-2-(3-methoxyphenyl)ethan-1-ol 
• 26767-10-2 2-(3-methoxyphenyl)glyoxylic acid 

Relevant articles and documents

ANTIHYPERTENSIVE POLYOL COMPOUND AND DERIVATIVE THEREOF

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Ru-MACHO-Catalyzed Highly Chemoselective Hydrogenation of α-Keto Esters to 1,2-Diols or α-Hydroxy Esters

A ruthenium pincer catalyst has been shown to be highly effective for the hydrogenation of a wide range of α-keto esters, affording either diols or hydroxy esters depending on the choice of reaction conditions. Strong base, high temperature, and pressure favor the formation of diols whilst the opposite is true for the hydroxy esters.

One-pot synthesis of enantiomerically pure 1, 2-diols: Asymmetric reduction of aromatic α-oxoaldehydes catalysed by Candida parapsilosis ATCC 7330

A facile and simple one-pot method was developed to produce a series of optically active (S)-1-phenyl-1,2-ethanediols with good yields (up to 70%) and high enantiomeric excess (>99%) via asymmetric reduction of various substituted aromatic α-oxoaldehydes using Candida parapsilosis ATCC 7330.