1,7-OCTADIYNE
1,7-OCTADIYNE Basic information
- Product Name:
- 1,7-OCTADIYNE
- Synonyms:
-
- 1,7-OCTADIYNE
- octa-1,7-diyne
- 1,7-Octadiyne (6CI, 7CI, 8CI, 9CI)
- 1,7-Octadiyne,98%
- 1,7-Dctadiyne
- 1,7-Octanediyne
- Octane-1,7-diyne
- 1,7-Octadiyne,99%
- CAS:
- 871-84-1
- MF:
- C8H10
- MW:
- 106.17
- EINECS:
- 212-815-0
- Product Categories:
-
- Acetylenes
- Acetylenic Hydrocarbons
- Alkynes
- Organic Building Blocks
- Terminal
- Mol File:
- 871-84-1.mol
1,7-OCTADIYNE Chemical Properties
- Melting point:
- 27°C (estimate)
- Boiling point:
- 135-136 °C (lit.)
- Density
- 0.8 g/mL at 25 °C (lit.)
- refractive index
- n20/D 1.446(lit.)
- Flash point:
- 74 °F
- storage temp.
- 2-8°C
- solubility
- Not miscible or difficult to mix.
- form
- Liquid
- Specific Gravity
- 0.817
- color
- Clear colorless to faintly yellow
- BRN
- 1697275
- CAS DataBase Reference
- 871-84-1(CAS DataBase Reference)
- EPA Substance Registry System
- 1,7-Octadiyne (871-84-1)
Safety Information
- Hazard Codes
- Xi
- Risk Statements
- 10-36/37/38
- Safety Statements
- 16-26-36/37/39
- RIDADR
- UN 3295 3/PG 3
- WGK Germany
- 3
- TSCA
- Yes
- HazardClass
- 3
- PackingGroup
- III
- HS Code
- 29012990
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
- Language:English Provider:ALFA
1,7-OCTADIYNE Usage And Synthesis
Chemical Properties
clear colorless to faintly yellow liquid
Uses
1,7-Octadiyne is an useful bifunctional chain extension unit. It participates in the formation of uranium(IV) vinyl complexes. It reacts with frustrated Lewis pair P(o-tolyl)3/B(C6F5)3 by acetylene C-C coupling to yield the zwitterionic product. It undergoes the reductive cyclization during reaction with Re2Cl4(?-dppm)2 (dppm = Ph2PCH2PPh2) and affords quadruply bonded dirhenium(III) complex Re2Cl3(?,η2-C8H7)(?-dppm)2.
General Description
1,7-Octadiyne is a terminal bis-alkyne and participates in the formation of uranium(IV) vinyl complexes. It reacts with frustrated Lewis pair P(o-tolyl)3/B(C6F5)3 by acetylene C-C coupling to yield the zwitterionic product. It undergoes the reductive cyclization during reaction with Re2Cl4(μ-dppm)2 (dppm = Ph2PCH2PPh2) and affords quadruply bonded dirhenium(III) complex Re2Cl3(μ,η2-C8H7)(μ-dppm)2.
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