54364-60-2

Basic information

• Product Name: (7Z,9E)-dodeca-7,9-dienol
• Synonyms: (7Z,9E)-dodeca-7,9-dienol;(7E,9Z)-7,9-Dodecadien-1-ol;(Z,E)-7,9-Dodecadien-1-ol;7,9-Dodecadien-1-ol, (7E,9Z)-;Einecs 259-126-1
• CAS NO: 54364-60-2
• Molecular Formula: C₁₂H₂₂O
• Molecular Weight: 182.30248
• EINECS: 259-126-1
• Mol File: 54364-60-2.mol
• Article Data: 12

Chemical Properties

• Boiling Point: 281°C at 760 mmHg
• Flash Point: 107°C
• Appearance: /
• Density: 0.862g/cm³
• Vapor Pressure: 0.000437mmHg at 25°C
• Refractive Index: 1.473
• PKA: 15.19±0.10(Predicted)
• CAS DataBase Reference: (7Z,9E)-dodeca-7,9-dienol(CAS DataBase Reference)
• NIST Chemistry Reference: (7Z,9E)-dodeca-7,9-dienol(54364-60-2)
• EPA Substance Registry System: (7Z,9E)-dodeca-7,9-dienol(54364-60-2)

Safety Data

• Hazardous Substances Data: 54364-60-2(Hazardous Substances Data)

Usage

Synthesis Reference(s)

Tetrahedron Letters, 24, p. 2513, 1983 DOI: 10.1016/S0040-4039(00)81969-3

InChI:InChI=1/C12H22O/c1-2-3-4-5-6-7-8-9-10-11-12-13/h3-6,13H,2,7-12H2,1H3/b4-3+,6-5-

Upstream product

• 22054-13-3 7-hydroxyheptanal 
• 7348-72-3 trans-Pent-2-enyl(triphenyl)phosphonium bromide 
• 95451-60-8 isopropyl (E)-3,8-nonadienoate 
• 108529-76-6 (2E)-2,8-nonadienal 
• 96754-52-8 (E)-9-(Tetrahydro-pyran-2-yloxy)-non-2-enal 
• 70979-87-2 (Z)-hept-4-en-2-yn-1-ol 
• 67818-17-1 (E)-2,(Z)-4-heptadien-1-yl acetate 
• 70979-88-3 (2E,4Z)-hepta-2,4-dien-1-ol 
• 306748-87-8 1,7E,9Z-Dodecatrien-4-ol 
• 306748-86-7 Methyl 4E,7Z-nonadienoate 
• 66471-41-8 4E,6Z-Nonadien-1-ol 
• 170753-58-9 dodeca-1,7E,9Z-triene 
• 76934-43-5 (7E,9Z)-2-((dodec-7,9-dien-1-yl)oxy)tetrahydro-2H-pyran 
• 54068-75-6 (Z)-1-iodobut-1-ene 

Downstream Products

• 54364-62-4 (7E,9Z)-7,9-dodecadien-1-yl acetate 
• 54364-63-5 (E,Z)-7,9-dodecadienyl acetate 

Relevant articles and documents

A STEREOSPECIFIC SYNTHESIS OF CONJUGATED (E,Z)-AND (E,E)-ALKADIENES BY THE PALLADIUM-CATALYZED REACTION OF (E)-1-ALKENYLBORONIC ACIDS AND 1-ALKENYL IODIDES

The reaction of (E)-1-alkenylboronic acids with (Z)-or(E)-1-alkenyl iodides in the presence of a catalytic amount of tetrakis(triphenylphosphine)-palladium and sodium hydroxide gave the corresponding conjugated (E,Z)-or (E,E)-alkadienes with high stereospecificity.

Economical synthesis of grapevine moth sex pheromone

-

Ozonolysis of alkenes and study of reactions of polyfunctional compounds: LXII. New synthetic route to 7E,9Z-dodecadien-1-yl acetate, pheromone of the leaf roller moth (Lobesia botrana)

Proceeding from the product of the partial ozonolysis of 1,4-cyclohexadiene, methyl 6-oxo-4E-hexenoate, a new synthetic route was developed to 7E,9Z-dodecadienyl acetate, pheromone of the leaf roller moth (Lobesia botrana).