5638-26-6

Basic information

• Product Name: 1,5-HEPTADIEN-4-OL
• Synonyms: 1,5-HEPTADIEN-4-OL
• CAS NO: 5638-26-6
• Molecular Formula: C₇H₁₂O
• Molecular Weight: 112.17
• Mol File: 5638-26-6.mol
• Article Data: 14

Chemical Properties

• Boiling Point: 160.13°C (estimate)
• Flash Point: 63.6°C
• Appearance: /
• Density: 0.8610
• Vapor Pressure: 0.7mmHg at 25°C
• Refractive Index: 1.4510
• CAS DataBase Reference: 1,5-HEPTADIEN-4-OL(CAS DataBase Reference)
• NIST Chemistry Reference: 1,5-HEPTADIEN-4-OL(5638-26-6)
• EPA Substance Registry System: 1,5-HEPTADIEN-4-OL(5638-26-6)

Safety Data

• Hazardous Substances Data: 5638-26-6(Hazardous Substances Data)

Usage

Synthesis Reference(s)

Tetrahedron Letters, 25, p. 6017, 1984 DOI: 10.1016/S0040-4039(01)81748-2

InChI:InChI=1/C7H12O/c1-3-5-7(8)6-4-2/h3-4,6-8H,1,5H2,2H3

Upstream product

• 24581-03-1 (5E)-hepta-1,5-dien-4-ol 
• 106-95-6 allyl bromide 
• 123-73-9 crotonaldehyde 
• 556-56-9 allyl iodid 
• 107-31-3 Methyl formate 
• 18925-10-5 allylzinc bromide 
• 688-61-9 Triallylborane 
• 53317-08-1 9-allyl-9-bora-bicyclo[3.3.1]nonane 
• 7393-43-3 tetraallyl tin 
• 81430-05-9 2-allyl-1,2-oxaborolane 
• 60-29-7 diethyl ether 
• 107-05-1 3-chloroprop-1-ene 
• 24850-33-7 allyltributylstanane 

Downstream Products

• 2196-23-8 1,3,5-heptatriene 
• 44607-51-4 trans-1,3,6-heptatriene 
• 55758-72-0 cis-1,3,6-heptatriene 
• 589-55-9 heptan-4-ol 

Relevant articles and documents

Bismuth chloride mediated allylation of carbonyl compounds in aqueous media: A mechanistic investigation

The bismuth chloride mediated, aluminum promoted aqueous Barbier type coupling of allyl unit with carbonyl compounds which gives the corresponding homoallyl alcohol is studied. The transient in situ generated allylbismuth(III) bromide intermediate was stu

Highly efficient synthesis of homoallylic alcohols and amines via allylation of aldehydes and imines catalyzed by ZrOCl2·8H2O in water

The allylation of aldehydes and imines has efficiently been carried out by treatment with allyltributylstannane in the presence of a catalytic amount of ZrOCl2·8H2O in water to form the corresponding homoallylic alcohols and amines,

ROMPgel supported allylboronate: A purification-free method for the preparation of homoallylic alcohols

Allylboration of various aldehydes was carried out by a ROMPgel supported allylboronate. Filtration and evaporation gave the corresponding homoallylic alcohols in high yield and purity (>95%).