78649-50-0

Basic information

• Product Name: 1-(3'-methylphenyl)-1,2-dihydroxyethane
• Synonyms: 1-(3'-methylphenyl)-1,2-dihydroxyethane
• CAS NO: 78649-50-0
• Molecular Weight: 152.193
• Mol File: 78649-50-0.mol
• Article Data: 13

Chemical Properties

• CAS DataBase Reference: 1-(3'-methylphenyl)-1,2-dihydroxyethane(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(3'-methylphenyl)-1,2-dihydroxyethane(78649-50-0)
• EPA Substance Registry System: 1-(3'-methylphenyl)-1,2-dihydroxyethane(78649-50-0)

Safety Data

• Hazardous Substances Data: 78649-50-0(Hazardous Substances Data)

Upstream product

• 100-80-1 3-methylstyrene 
• 766-82-5 1-ethynyl-3-methyl-benzene 
• 591-17-3 meta-bromotoluene 
• 620-23-5 m-tolyl aldehyde 
• 34867-87-3 spirocyclobutylmalonoyl peroxide 
• 704898-29-3 3-methylstyrene oxide 

Downstream Products

• 138232-28-7 (S)-1-(3-methylphenyl)ethane-1,2-diol 
• 620-23-5 m-tolyl aldehyde 
• 387337-84-0 2-phenyl-4-m-tolyl-[1,3]dioxolane 
• 14471-61-5 6-bromo-3-(3-methyl-benzyl)-1,1-dioxo-1,2,3,4-tetrahydro-1λ⁶-benzo[1,2,4]thiadiazine-7-sulfonic acid amide 
• 14471-81-9 3-(3-methyl-benzyl)-1,1-dioxo-6-trifluoromethyl-1,2,3,4-tetrahydro-1λ⁶-benzo[1,2,4]thiadiazine-7-sulfonic acid amide 
• 14331-58-9 6-chloro-3-(3-methyl-benzyl)-1,1-dioxo-1,2,3,4-tetrahydro-1λ⁶-benzo[1,2,4]thiadiazine-7-sulfonic acid amide 

Relevant articles and documents

ANTIHYPERTENSIVE POLYOL COMPOUND AND DERIVATIVE THEREOF

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Direct, high-yielding, one-step synthesis of vic-diols from aryl alkynes

An unprecedented, high yielding, direct, one-step synthesis of vic-diols from alkynes has been developed via metal-free, open-to-air dihydroboration with ammonia borane. The electronics of the alkyne and the reaction stoichiometry are critical for obtaining optimal yields of the 1,2-diol.

Cp2TiCl2-catalyzed cycloboration of α-olefins with PhBCl2in the synthesis of 2-alkyl(aryl,benzyl)-1-phenylboriranes

A one-pot method for the synthesis of 2-alkyl(aryl, benzyl)-1-phenylboriranes has been developed via the reaction of α-olefins with PhBCl2in the presence of Cp2TiCl2as the catalyst. The method implies the formation of boriranes as the result of transmetalation of titanacyclopropane intermediates generated in the reaction of α-olefins with Cp2TiCl2. Individual 1-phenyl-2-substituted boriranes were isolated and their structures confirmed by NMR spectral methods.