51756-19-5

Basic information

• Product Name: 2-Methyl-1-nonen-3-one
• Synonyms: 2-Methyl-1-nonen-3-one
• CAS NO: 51756-19-5
• Molecular Formula: C₁₀H₁₈O
• Molecular Weight: 154.25
• Mol File: 51756-19-5.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 198.7°C at 760 mmHg
• Flash Point: 71.8°C
• Appearance: /
• Density: 0.828g/cm³
• Vapor Pressure: 0.355mmHg at 25°C
• Refractive Index: 1.427
• CAS DataBase Reference: 2-Methyl-1-nonen-3-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Methyl-1-nonen-3-one(51756-19-5)
• EPA Substance Registry System: 2-Methyl-1-nonen-3-one(51756-19-5)

Safety Data

• Hazardous Substances Data: 51756-19-5(Hazardous Substances Data)

Usage

InChI:InChI=1/C9H16O/c1-3-5-6-7-8-9(10)4-2/h4H,2-3,5-8H2,1H3

Upstream product

• 52500-37-5 2-methylnon-1-en-3-ol 
• 111-71-7 heptanal 
• 111-25-1 1-bromo-hexane 
• 1184-78-7 trimethylamine-N-oxide 
• 85199-51-5 2-Nitro-3-nonanone 
• 88226-44-2 Acetic acid 2-methyl-2-nitro-3-oxo-nonyl ester 
• 88226-37-3 1-Hydroxy-2-methyl-2-nitro-nonan-3-one 
• 463-49-0 1,2-propanediene 
• 1116-73-0 trihexylaluminium 
• 920-46-7 Methacryloyl chloride 
• 93233-76-2 (1-Isopropenyl-1-methoxy-heptylsulfanyl)-benzene 
• 83135-37-9 allyl 2-methyl-2-heptanylpropanoate 
• 88226-49-7 Acetic acid 2-methyl-3-oxo-nonyl ester 
• 51756-17-3 (2-methoxycarbonyl-2-methyl-3-oxo-nonyl)-trimethyl-ammonium; iodide 

Downstream Products

• 123718-30-9 3-hexyl-2,2,4-trimethyl-8-phenyl-1,6,8-triaza<4.3.0>bicyclonon-3-ene-7,9-dione 
• 115819-58-4 3-hexyl-2,4-dimethyl-4-phenylselenopent-1-en-3-ol 

Relevant articles and documents

A New Synthesis of Substituted Dienes and its Application to an Alkylated Taxane Model System

A new synthesis of highly substituted dienes using LiCMe2SePh is reported, along with its application to the synthesis of the taxane model compound 8,12,15,15-tetramethyltricyclo3,8>pentadecane

A NEW SYNTHESIS OF α-METHYLENE CARBONYL COMPOUNDS

α-Methylene carbonyl compounds are regioselectively prepared by the reaction of α-nitroketones or α-nitroesters with 37percent formaldehyde in the presence of a catalytic amount of weak bases followed by acetylation, denitration with Bu3SnH, and elimination of acetic acid.