1,5-Hexadiene
1,5-Hexadiene is the organic compound with the formula (CH2)2(CH=CH2)2. It is a colorless, volatile liquid. It is used as a crosslinking agent and precursor to a variety of other compounds.
 | |
| Names | |
|---|---|
| Preferred IUPAC name
Hexa-1,5-diene | |
| Other names
diallyl, biallyl, α,ω-Hexadiene | |
| Identifiers | |
3D model (JSmol) |
|
| ChemSpider | |
| ECHA InfoCard | 100.008.869 |
| EC Number |
|
PubChem CID |
|
| UNII | |
CompTox Dashboard (EPA) |
|
| |
| |
| Properties | |
| C6H10 | |
| Molar mass | 82.146 g·mol−1 |
| Appearance | colorless liquid |
| Boiling point | 59–60 °C (138–140 °F; 332–333 K) |
| Hazards | |
| GHS pictograms |    |
| GHS Signal word | Danger |
GHS hazard statements |
H225, H304, H315, H319, H335, H336 |
| P210, P233, P240, P241, P242, P243, P261, P264, P271, P280, P301+310, P302+352, P303+361+353, P304+340, P305+351+338, P312, P321, P331, P332+313, P337+313, P362, P370+378, P403+233, P403+235, P405 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Synthesis
1,5-Hexadiene is produced commercially by the ethenolysis of 1,5-cyclooctadiene:[1]
- (CH2CH=CHCH2)2 + 2 CH2=CH2 → 2 (CH2)2CH=CH2
The catalyst is derived from Re2O7 on alumina.
A laboratory-scale preparation involves reductive coupling of allyl chloride using magnesium:[2]
- 2 ClCH2CH=CH2 + Mg → (CH2)2(CH=CH2)2 + MgCl2
gollark: Well, this is irritating, APPARENTLY the packets are very mean and will not go both directions.
gollark: So clear, well-formatted and comprehensible.
gollark: Some of the documentation references Ethereum, which they appear to be using somehow‽
gollark: Because something something scarcity and *obviously* making your addresses scarce worked well for IPv4!
gollark: > There are two semantic patterns, transfer and retain. In transfer semantics, the caller "gives" a use count to the callee, which "gives back" any return. For instance, if I haveAre they implementing Rust as a convention in C with weird terminology?
References
- Lionel Delaude; Alfred F. Noels (2005). "Metathesis". Kirk-Othmer Encyclopedia of Chemical Technology. Weinheim: Wiley-VCH. doi:10.1002/0471238961.metanoel.a01.
- Amos Turk; Henry Chanan (1947). "Biallyl". Org. Synth. 27: 7. doi:10.15227/orgsyn.027.0007.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.