Suberoyl chloride
Suberoyl chloride is an organic compound with the formula (CH2)6(COCl)2. It is the diacid chloride derivative of suberic acid. It is a colorless liquid although aged samples appear yellow or even brown.
 | |
 | |
| Names | |
|---|---|
| IUPAC name
Octanedioyl dichloride | |
| Other names
Suberoyl dichloride; Suberic acid chloride | |
| Identifiers | |
3D model (JSmol) |
|
| ChemSpider | |
| ECHA InfoCard | 100.156.463 |
PubChem CID |
|
CompTox Dashboard (EPA) |
|
| |
| |
| Properties | |
| C8H12Cl2O2 | |
| Molar mass | 211.08 g·mol−1 |
| Density | 1.172 g/cm3 |
| Boiling point | 162–163 °C (324–325 °F; 435–436 K) |
| Reacts with water | |
| Hazards | |
| GHS pictograms |  |
| GHS Signal word | Danger |
GHS hazard statements |
H314, H318 |
| P260, P264, P280, P301+330+331, P303+361+353, P304+340, P305+351+338, P310, P321, P363, P405, P501 | |
| Flash point | 110 °C (230 °F; 383 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Uses
Suberoyl chloride is used as a reagent to synthesize hydroxyferrocifen hybrid compounds that have antiproliferative activity against triple negative breast cancer cells. It is also used as a cross-linking agent to cross-link chitosan membranes, and also improves the membrane's integrity.[1]
References
- "Suberoyl chloride". Alfa Aesar. Retrieved 16 April 2019.
External links
Diacyl chlorides (-COCl)2 | ||
|---|---|---|
|  | |
Category:Acyl chlorides | ||
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.