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| Names | |||
|---|---|---|---|
|
Preferred IUPAC name
1,4-diisocyanobutane | |||
|
Systematic IUPAC name
1,4-diisocyanobutane | |||
| Identifiers | |||
3D model (
JSmol)
|
|||
| ChemSpider | |||
PubChem
CID
|
|||
| |||
| |||
| Properties | |||
| C6H8N2 | |||
| Molar mass | 108.144 g·mol−1 | ||
| Hazards | |||
| GHS labelling: | |||
[1]
| |||
| Danger [1] | |||
| H301, H311, H331 [1] | |||
| P261, P264, P270, P271, P280, P301+P316, P302+P352, P304+P340, P316, P321, P330, P361+P364, P403+P233, P405, P501 [1] | |||
| Related compounds | |||
Related compounds
|
|||
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
| |||
1,4-Diisocyanobutane is an organic compound. Its structural formula is CN(CH2)4NC, which similar to adiponitrile but with carbon and nitrogen of cyanide groups switching places. It has been used as a ligand in the formation of organometallic complexes, such as with rhodium - [Rh2(CNC8H14NC)42+. [2]
- ^ a b c d PubChem. "1,4-Diisocyanobutane". pubchem.ncbi.nlm.nih.gov. Retrieved 2022-07-29.
- ^ Yaneff, P.V.; Powell, J. (1979). "Dinuclear complexes of rhodium(I) containing diisocyanide ligands and some of their phosphine derivatives". Journal of Organometallic Chemistry. 179: 101–113. doi: 10.1016/S0022-328X(00)87800-6.
 | This article about an organic compound is a stub. You can help Wikipedia by expanding it. |
|
| |||
| |||
| Names | |||
|---|---|---|---|
|
Preferred IUPAC name
1,4-diisocyanobutane | |||
|
Systematic IUPAC name
1,4-diisocyanobutane | |||
| Identifiers | |||
3D model (
JSmol)
|
|||
| ChemSpider | |||
PubChem
CID
|
|||
| |||
| |||
| Properties | |||
| C6H8N2 | |||
| Molar mass | 108.144 g·mol−1 | ||
| Hazards | |||
| GHS labelling: | |||
|
[1]
| |||
| Danger [1] | |||
| H301, H311, H331 [1] | |||
| P261, P264, P270, P271, P280, P301+P316, P302+P352, P304+P340, P316, P321, P330, P361+P364, P403+P233, P405, P501 [1] | |||
| Related compounds | |||
Related compounds
|
|||
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
| |||
1,4-Diisocyanobutane is an organic compound. Its structural formula is CN(CH2)4NC, which similar to adiponitrile but with carbon and nitrogen of cyanide groups switching places. It has been used as a ligand in the formation of organometallic complexes, such as with rhodium - [Rh2(CNC8H14NC)42+. [2]
- ^ a b c d PubChem. "1,4-Diisocyanobutane". pubchem.ncbi.nlm.nih.gov. Retrieved 2022-07-29.
- ^ Yaneff, P.V.; Powell, J. (1979). "Dinuclear complexes of rhodium(I) containing diisocyanide ligands and some of their phosphine derivatives". Journal of Organometallic Chemistry. 179: 101–113. doi: 10.1016/S0022-328X(00)87800-6.
|
| This article about an organic compound is a stub. You can help Wikipedia by expanding it. |