| |
| Names | |
|---|---|
|
Preferred IUPAC name
Octanoyl chloride | |
| Other names
Capryloyl chloride; n-Octanoyl chloride; Caprylic acid chloride
| |
| Identifiers | |
3D model (
JSmol)
|
|
| ECHA InfoCard | 100.003.538 |
PubChem
CID
|
|
| UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| Properties | |
| C8H15ClO | |
| Molar mass | 162.66 g·mol−1 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
| |
Octanoyl chloride is an eight-carbon acyl chloride with a straight-chain structure that is used as a reagent in organic synthesis. [1] [2]
References
- ^ "Octanoyl chloride". Sigma-Aldrich. Retrieved 1 July 2017.
- ^ "Octanoyl Chloride". PubChem. Retrieved 1 July 2017.
|
| |
| Names | |
|---|---|
|
Preferred IUPAC name
Octanoyl chloride | |
| Other names
Capryloyl chloride; n-Octanoyl chloride; Caprylic acid chloride
| |
| Identifiers | |
3D model (
JSmol)
|
|
| ECHA InfoCard | 100.003.538 |
PubChem
CID
|
|
| UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| Properties | |
| C8H15ClO | |
| Molar mass | 162.66 g·mol−1 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
| |
Octanoyl chloride is an eight-carbon acyl chloride with a straight-chain structure that is used as a reagent in organic synthesis. [1] [2]
References
- ^ "Octanoyl chloride". Sigma-Aldrich. Retrieved 1 July 2017.
- ^ "Octanoyl Chloride". PubChem. Retrieved 1 July 2017.