120872-41-5

Basic information

• Product Name: 1-Nonene, 1-methoxy-
• CAS NO: 120872-41-5
• Molecular Formula: C10H20O
• Molecular Weight: 156.268
• Mol File: 120872-41-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-Nonene, 1-methoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Nonene, 1-methoxy-(120872-41-5)
• EPA Substance Registry System: 1-Nonene, 1-methoxy-(120872-41-5)

Safety Data

• Hazardous Substances Data: 120872-41-5(Hazardous Substances Data)

Downstream Products

• 138982-77-1 trans-3-Heptyl-5-(2-phenylvinyl)-1,2,4-trioxolane 
• 138982-77-1 cis-3-Heptyl-5-(2-phenylvinyl)-1,2,4-trioxolane 
• 122744-73-4 Dihydro-cis,cis-3-heptyl-5,6-diphenyl-1,2,4,5-trioxazine 
• 122744-73-4 Dihydro-trans,trans-3-heptyl-5,6-diphenyl-1,2,4,5-trioxazine 
• 138982-79-3 trans-3-Heptyl-5-(2,2-diphenylvinyl)-1,2,4-trioxolane 
• 138982-79-3 cis-3-Heptyl-5-(2,2-diphenylvinyl)-1,2,4-trioxolane 
• 130012-03-2 (3S,5S)-3-Heptyl-5-(2-trifluoromethyl-phenyl)-[1,2,4]trioxolane 
• 130012-02-1 (3R,5S)-3-Heptyl-5-(2-trifluoromethyl-phenyl)-[1,2,4]trioxolane 
• 122744-76-7 Dihydro-3-heptyl-5,6,6-triphenyl-1,2,4,5-trioxazine 
• 122744-75-6 (3S,6S)-5-Benzyl-3,6-diheptyl-[1,2,4,5]trioxazinane 
• 122744-75-6 (3R,6S)-5-Benzyl-3,6-diheptyl-[1,2,4,5]trioxazinane 
• 107-31-3 Methyl formate 
• 130011-78-8 trans-3-heptyl-5-methoxy-1,2,4-trioxolane 
• 130011-72-2 cis-3-heptyl-5-methoxy-1,2,4-trioxolane 

Relevant articles and documents

Ozonolysis of Vinyl Ethers in Solution and on Polyethylene

Ozonolyses of the vinyl ethers 1a-f in methanol afforded almost exclusively the corresponding α-methoxy hydroperoxides 4, suggesting the preferred formation of the carbonyl oxides 2.In aprotic solvents including methyl formate, the predominant modes of decay of the carbonyl oxides 2 were cyclodimerization, reduction, and rearrangement, yet no ozonide formation.By contrast, ozonolyses of 1a-f on polyethylene gave the α-methoxy-substituted ozonides 14 in fair yields.Ozonolyzes of 1a-f in the presence of added carbonyl compounds 6 in methylene chloride or ether yielded the corresponding cross ozonides.Judged from the ozonide yields, the reactivities of the carbonyl compounds follow the sequence: (ClCH2)2C=O > ClCH2COCH3 > (CH3)2C=O and 2-CF3C6H4CHO > PhCHO.