17679-92-4

Basic information

• Product Name: 1-OCTEN-3-YNE
• Synonyms: 1-Octene-3-yne;n-C4H9CequivCCH=CH2;1-OCTEN-3-YNE
• CAS NO: 17679-92-4
• Molecular Formula: C₈H₁₂
• Molecular Weight: 108.18
• Mol File: 17679-92-4.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 133.85°C
• Flash Point: 24.9 °C
• Appearance: /
• Density: 0.7749
• Vapor Pressure: 8.4mmHg at 25°C
• Refractive Index: 1.4592
• CAS DataBase Reference: 1-OCTEN-3-YNE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-OCTEN-3-YNE(17679-92-4)
• EPA Substance Registry System: 1-OCTEN-3-YNE(17679-92-4)

Safety Data

• Hazardous Substances Data: 17679-92-4(Hazardous Substances Data)

Usage

Also known as

Methylidenecyclohexane

Physical state

Colorless liquid

Odor

Pungent

Flammability

Highly flammable

Uses

Flavoring agent in food products
Building block in chemical production
Solvent in organic reactions
Reagent in organic synthesis

Pest control properties

Insecticidal and fungicidal

Agricultural applications

Useful due to pest control properties

Handling precautions

Handle with caution due to flammability and potential hazards

InChI:InChI=1/C8H12/c1-3-5-7-8-6-4-2/h3H,1,4,6,8H2,2H3

Upstream product

• 628-71-7 1-Heptyne 
• 32359-01-6 hexenylmagnesium bromide 
• 593-60-2 Vinyl bromide 
• 693-02-7 hex-1-yne 
• 64-17-5 ethanol 
• 109-65-9 1-bromo-butane 
• 51065-64-6 6-methyl-2-heptyne 
• 37050-06-9 7-methyl-3-octyne 
• 1119-65-9 hept-2-yne 
• 15232-76-5 oct-3-yne 
• 2586-89-2 hept-3-yne 
• 764-35-2 2-Hexyne 
• 1942-46-7 5-decyne 
• 2809-67-8 oct-2-yne 

Downstream Products

• 596815-70-2 1-(4'-methylphenyl)-2-butylnona-2,3-dien-1-one 
• 111-66-0 oct-1-ene 
• 96975-17-6 2-Butyl-1,1,1,6,6,6-hexaphenyl-hexadien-(2,3) 
• 111-65-9 octane 

Relevant articles and documents

Ni-Catalyzed Decarboxylative Silylation of Alkynyl Carbonates: Access to Chiral Allenes via Enantiospecific Conversions

A Ni-mediated decarboxylative silylation of alkynyl cyclic carbonates used as versatile propargylic surrogates is reported affording a wide range of highly substituted 2,3- and 3,4-allenol products in good yields. The formal cross-coupling between a tentative intermediate Ni(allenyl) and the silyl reagent was further extended to enantiospecific conversions providing access to chiral allene synthons. This protocol marks the first Ni-catalyzed propargylic silylation proceeding through an SN2′ manifold.

Control of the Propargylic Radical Stabilization by Carbon-Chain Length in Manganese(III)-Mediated Reactions of 1-Alken-3-ynes. - A Facile Synthetic Way to Long-Chain 4-Acetoxy-5-alkynoic Acids

By investigation of reactions of 1-alken-3-ynes RCC-CH=CH2 4 with acetic acid/ acetic anhydride, mediated by manganese(III) acetate, it has been found that the stabilization of propargylic radical adducts depends on the carbon-chain length of R in 4.R=C8H17 is shown to be the "critical" chain length when ligand transfer reaction appears to be the only way of stabilization of intermediates, thus providing a facile one-step access to long-chain 4-acetoxy-5-alkynoic caids.The dependence of the product ratios on the AcOH/Ac2O ratio has also been demonstrated. Key Words: 1-Alken-3-ynes / Manganese(III) acetate / Propargyl radical / Ligand-transfer reaction / Electron-transfer reaction