53544-43-7

Basic information

• Product Name: 1-but-3-en-1-ylcyclopentanol
• Synonyms: 1-(But-3-en-1-yl)cyclopentanol; cyclopentanol, 1-(3-buten-1-yl)-
• CAS NO: 53544-43-7
• Molecular Formula: C₉H₁₆O
• Molecular Weight: 140.2227
• Mol File: 53544-43-7.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 198.2°C at 760 mmHg
• Flash Point: 78.7°C
• Density: 0.935g/cm³
• Vapor Pressure: 0.0923mmHg at 25°C
• Refractive Index: 1.484
• CAS DataBase Reference: 1-but-3-en-1-ylcyclopentanol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-but-3-en-1-ylcyclopentanol(53544-43-7)
• EPA Substance Registry System: 1-but-3-en-1-ylcyclopentanol(53544-43-7)

Safety Data

• Hazardous Substances Data: 53544-43-7(Hazardous Substances Data)

Upstream product

• 5162-44-7 1-bromo-4-butene 
• 120-92-3 cyclopentanone 
• 7103-09-5 4-but-1-enylmagnesium bromide 

Downstream Products

• 1620886-71-6 (Z)-2-(1-oxaspiro[4.4]nonan-2-ylmethyl)-3-chloro-3-phenylacrylamide 
• 175-93-9 spiro[4.4]nonane 
• 873-12-1 Spiro<4.4>non-1-en 
• 4551-51-3 cis-hydrindane 
• 3296-50-2 trans-octahydro-1H-indene 
• 119681-02-6 2-Allyl-1-oxa-spiro[2.4]heptane 
• 119681-01-5 1-(3'-butenyl)-1,2-epoxycyclopentane 
• 100238-92-4 2-Bromomethyl-1-oxa-spiro[4.4]nonane 

Relevant articles and documents

A Simple Iterative Approach to the Synthesis of cis-cisoid-cis-Tricyclo2,6>undecane Carbon Skeleton

In an iterative synthesis utilizing only four reagents, cyclopentanone has been converted into cis-cisoid-cis-tricyclo2,6>undecane carbon skeleton in high yield.

Organocatalytic synthesis of polysubstituted tetrahydrofurans from alkenes

A novel, organocatalytic and environmentally friendly protocol for the synthesis of polysubstituted tetrahydrofurans from trivial starting materials has been described. By employing 2,2,2-trifluoroacetophenone-mediated oxidation, which utilizes H2O2 as a green oxidant, we introduce a sustainable procedure that embraces the principles of green chemistry for the production of substituted tetrahydrofurans in high to excellent yields and tolerates a wide range of substitution patterns.

Synthesis of spiranic heterocycles by induced decomposition of unsaturated peroxides

Induced decomposition of unsaturated peroxides in a good hydrogen-donor solvent leads to the functionalization of the latter.If the peroxide contains a cycle on the carbon next to the O-O bond, the reaction gives spirans with an oxiran, an oxetan or a tetrahydrofuran ring in good or even excellent yields.Keywords: unsaturated peroxide / spiranic heterocycles / induced decomposition / homolytic intramolecular substitution / radical addition