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About This Item
Linear Formula:
CH3CH2C≡C(CH2)4C≡CCH2CH3
CAS Number:
Molecular Weight:
162.27
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
Assay
97%
refractive index
n20/D 1.465 (lit.)
bp
55-58 °C/0.5 mmHg (lit.)
density
0.809 g/mL at 25 °C (lit.)
SMILES string
CCC#CCCCCC#CCC
InChI
1S/C12H18/c1-3-5-7-9-11-12-10-8-6-4-2/h3-4,9-12H2,1-2H3
InChI key
SLQXYOMUNKJHRV-UHFFFAOYSA-N
General description
3,9-Dodecadiyne is an internal diyne that can undergo nickel-catalyzed cycloaddition with aryl nitriles to form pyridines.
Application
3,9-Dodecadiyne may be used as a monomer to prepare soluble hyperbranched poly(phenylenealkenes) via transition metal-catalyzed polycyclotrimerization. It may also be used as a starting material for preparing 1,2,3,4,9,10-hexaethyl-6,7,8,9-tetrahydroanthracene.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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New catalysts for polymerizations of substituted acetylenes.
Tang BZ, et al.
ACS Symp. Ser., 760 (2000)
Novel synthetic route to octasubstituted naphthalenes from four alkynes and one olefin unit via zirconacyclopentadienes and 1,2-diiodo-3,4,5,6-tetraalkylbenzene.
Zhou X, et al.
The Journal of Organic Chemistry, 69(13), 4559-4562 (2004)
A nickel-catalyzed route to pyridines.
McCormick MM, et al.
Journal of the American Chemical Society, 127(14), 5030-5031 (2005)
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