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| 1,6-HEPTADIYNE Basic information |
Product Name: | 1,6-HEPTADIYNE | Synonyms: | 1,6-HEPTADIYNE 98%;1,6-Heptadiyne, 97+%;1,6-Heptadiyne (6CI, 8CI, 9CI);Heptane-1,6-diyne;1,6-Heptadiyne,98%;1,6-HEPTADIYNE;1,6-HEPTADIYNE, 97%1,6-HEPTADIYNE, 97%1,6-HEPTADIYNE, 97%1,6-HEPTADIYNE, 97%;1,6-Heptadiyne> | CAS: | 2396-63-6 | MF: | C7H8 | MW: | 92.14 | EINECS: | 219-253-5 | Product Categories: | Industrial/Fine Chemicals;Acetylenes;Acetylenic Hydrocarbons;Alkynes;Organic Building Blocks;Terminal | Mol File: | 2396-63-6.mol | |
| 1,6-HEPTADIYNE Chemical Properties |
Melting point | -85 °C | Boiling point | 111.5 °C (lit.) | density | 0.805 g/mL at 25 °C (lit.) | refractive index | n20/D 1.441(lit.) | Fp | 49 °F | storage temp. | 2-8°C | form | Liquid | Specific Gravity | 0.805 | color | Clear yellow | Water Solubility | Insoluble in water. | BRN | 1731756 | CAS DataBase Reference | 2396-63-6(CAS DataBase Reference) | EPA Substance Registry System | 1,6-Heptadiyne (2396-63-6) |
Hazard Codes | F | Risk Statements | 11 | Safety Statements | 16-29-33 | RIDADR | UN 3295 3/PG 2 | WGK Germany | 2 | RTECS | MI5600000 | TSCA | Yes | HazardClass | 3 | PackingGroup | II | HS Code | 29012990 | Toxicity | dog,LD50,oral,3830mg/kg (3830mg/kg),GASTROINTESTINAL: NAUSEA OR VOMITINGLIVER: "HEPATITIS, FIBROUS (CIRRHOSIS, POST-NECROTIC SCARRING)"BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY),Federation Proceedings, Federation of American Societies for Experimental Biology. Vol. 19, Pg. 389, 1960. |
| 1,6-HEPTADIYNE Usage And Synthesis |
Chemical Properties | clear yellow liquid | Uses | 1,6-Heptadiyne may be used in the preparation of free-standing polymer films of poly(1,6-heptadiyne). 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. | 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. |
| 1,6-HEPTADIYNE Preparation Products And Raw materials |
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