1,6-HEPTADIYNE
1,6-HEPTADIYNE Basic information
- Product Name:
- 1,6-HEPTADIYNE
- Synonyms:
-
- 1,6-HEPTADIYNE, 97%1,6-HEPTADIYNE, 97%1,6-HEPTADIYNE, 97%1,6-HEPTADIYNE, 97%
- 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>
- 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.)
- Flash point:
- 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)
Safety Information
- 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.
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
- Language:English Provider:ALFA
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.
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- RARECHEM AQ A3 0170
- SALOR-INT L159891-1EA
- GOLFOMYCIN A