58046-43-8

Basic information

• Product Name: 4-ethyloct-1-en-3-ol
• Synonyms: 4-ethyloct-1-en-3-ol;4-Ethyl-1-octen-3-ol;Einecs 261-081-8
• CAS NO: 58046-43-8
• Molecular Formula: C₁₀H₂₀O
• Molecular Weight: 156.2652
• EINECS: 261-081-8
• Mol File: 58046-43-8.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 197.3°Cat760mmHg
• Flash Point: 71.9°C
• Appearance: /
• Density: 0.835g/cm³
• Vapor Pressure: 0.0975mmHg at 25°C
• Refractive Index: 1.442
• CAS DataBase Reference: 4-ethyloct-1-en-3-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-ethyloct-1-en-3-ol(58046-43-8)
• EPA Substance Registry System: 4-ethyloct-1-en-3-ol(58046-43-8)

Safety Data

• Hazardous Substances Data: 58046-43-8(Hazardous Substances Data)

Usage

InChI:InChI=1/C10H20O/c1-4-7-8-9(5-2)10(11)6-3/h6,9-11H,3-5,7-8H2,1-2H3

Upstream product

• 5877-42-9 4-ethyl-1-octyn-3-ol 
• 123-05-7 d,l-2-ethylhexanal 
• 1826-67-1 vinyl magnesium bromide 

Downstream Products

• 1361033-31-9 4-ethyl-1-(3-iodophenyl)octan-3-one 

Relevant articles and documents

Access to Saturated Thiocyano-Containing Azaheterocycles via Selenide-Catalyzed Regio-A nd Stereoselective Thiocyanoaminocyclization of Alkenes

An efficient route for the synthesis of saturated thiocyano-containing azaheterocycles by selenide-catalyzed regio-A nd stereoselective thiocyanoaminocyclization of alkenes is disclosed. The desired products were obtained in moderate to high yields under mild conditions. The generality of this method was elucidated by its efficient application in thiocyano oxycyclization of alkenes.

Ir-catalysed formation of C-F bonds. From allylic alcohols to α-fluoroketones

A novel iridium-catalysed tandem isomerisation/C-F bond formation from allylic alcohols and Selectfluor to prepare α-fluorinated ketones as single constitutional isomers is reported.