Recommended Products
Assay
97%
form
liquid
refractive index
n20/D 1.441 (lit.)
bp
111.5 °C (lit.)
density
0.805 g/mL at 25 °C (lit.)
storage temp.
2-8°C
SMILES string
C#CCCCC#C
InChI
1S/C7H8/c1-3-5-7-6-4-2/h1-2H,5-7H2
InChI key
RSPZSDWVQWRAEF-UHFFFAOYSA-N
Related Categories
General description
Polymerization of 1,6-heptadiyne using an insoluble Zeigler-Natta catalyst affords soluble polymer having six-membered ring containing polyene. Ruthenium(II)-catalyzed reaction of a substituted 1,6-heptadiyne with norbornene affords a tandem [2+ 2+ 2]/[4+2] cycloaddition product and a [2+ 2+2] cycloadduct. Cyclocopolymerization of 1,6-heptadiyne with dipropargyl ether under nitrogen atmosphere using KSCN, KBr and KI as initiators in N,N-dimethyl formamide has been studied.
Application
1,6-Heptadiyne may be used in the preparation of free-standing polymer films of poly(1,6-heptadiyne).
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Flam. Liq. 2
Storage Class Code
3 - Flammable liquids
WGK
WGK 2
Flash Point(F)
48.2 °F - closed cup
Flash Point(C)
9 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
Poly (1, 6-heptadiyne), a free-standing polymer film dopable to high electrical conductivity.
Journal of the American Chemical Society, 105(13), 4417-4431 (1983)
Simultaneous synthesis and doping of poly (1, 6-heptadiyne-co-dipropargyl ether) using ionic initiators.
Polymer, 43(6), 1781-1787 (2002)
Ruthenium-catalyzed tandem [2+ 2+ 2]/[4+ 2] cycloaddition of 1, 6-heptadiyne with norbornene.
Organometallics, 17(10), 1910-1912 (1998)
Molecules (Basel, Switzerland), 24(11) (2019-06-15)
Synthesis of 1,2,3-triazole-substituted coumarins and also 1,2,3-triazolyl or 1,2,3-triazolylalk-1-inyl-linked coumarin-2,3-furocoumarin hybrids was performed by employing the cross-coupling and copper catalyzed azide-alkyne cycloaddition reaction approaches. The synthesized compounds were evaluated for their in vitro antibacterial activity against Staphylococcusaureus, Bacilliussubtilis, Actinomycesviscosus and
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service