Chemistry:Octanoyl chloride
From HandWiki
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| Names | |
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| Preferred IUPAC name
Octanoyl chloride | |
| Other names
Capryloyl chloride; n-Octanoyl chloride; Caprylic acid chloride
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| Identifiers | |
3D model (JSmol)
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| ChEMBL | |
| ChemSpider | |
| EC Number |
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PubChem CID
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| UNII | |
| UN number | 1760 |
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| Properties | |
| C8H15ClO | |
| Molar mass | 162.66 g·mol−1 |
| Hazards | |
| GHS pictograms |   
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| GHS Signal word | Danger |
| H290, H315, H317, H318, H330 | |
| P234, P260, P261, P264, P264+265Script error: No such module "Preview warning".Category:GHS errors, P271, P272, P280, P284, P302+352, P304+340, P305+354+338Script error: No such module "Preview warning".Category:GHS errors, P316Script error: No such module "Preview warning".Category:GHS errors, P317Script error: No such module "Preview warning".Category:GHS errors, P320, P321, P332+317Script error: No such module "Preview warning".Category:GHS errors, P333+317Script error: No such module "Preview warning".Category:GHS errors, P362+364Script error: No such module "Preview warning".Category:GHS errors, P390, P403+233, P405, P406, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Tracking categories (test):
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". http://www.sigmaaldrich.com/catalog/product/aldrich/o4733?lang=en®ion=US. Retrieved 1 July 2017.
- ↑ "Octanoyl Chloride". https://pubchem.ncbi.nlm.nih.gov/compound/Octanoyl_chloride. Retrieved 1 July 2017.
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