332871-48-4

Basic information

• Product Name: 3-Octanone, 1-hydroxy-2-methyl-
• CAS NO: 332871-48-4
• Molecular Formula: C9H18O2
• Molecular Weight: 158.241
• Mol File: 332871-48-4.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 3-Octanone, 1-hydroxy-2-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Octanone, 1-hydroxy-2-methyl-(332871-48-4)
• EPA Substance Registry System: 3-Octanone, 1-hydroxy-2-methyl-(332871-48-4)

Safety Data

• Hazardous Substances Data: 332871-48-4(Hazardous Substances Data)

Upstream product

• 103941-98-6 2-methyloctane-1,3-diol 
• 50-00-0 formaldehyd 
• 3391-86-4 1-octen-3-ol 

Downstream Products

• 585-25-1 octane-2,3-dione 
• 15001-63-5 2-methyl-3-oxooctanal 

Relevant articles and documents

2-Iodoxybenzoic acid mediated facile conversion of 1,3-diols to 1,2-diketones by oxidative cleavage of the C-C bond

1,3-Diols undergo smooth oxidative cleavage of the C-C bond in the presence of 2-iodoxybenzoic acid (IBX) affording 1,2-diketones in excellent yields under mild conditions. Georg Thieme Verlag Stuttgart.

Development of new iron catalysts for the tandem isomerization-aldol condensation of allylic alcohols

(bda)Fe(CO)3 and (COT)Fe(CO)3 are shown to be excellent catalysts for the tandem isomerization-aldol reaction of allylic alcohols with aldehydes and to significantly increase the scope of this aldolization process, especially, in the

From allylic alcohols to aldols via a novel, tandem isomerization-condensation catalyzed by Fe(CO)5

Allylic alcohols react with aldehydes, in the presence of catalytic amounts of Fe(CO)5 and under irradiation, to give mainly aldol products. A small amount of ketone resulting from the classical isomerization process is also isolated. This new aldol-type reaction is a complete atom economy process occurring under neutral conditions.