Pimeloyl chloride
Pimeloyl chloride is a di-acyl chloride. It is used as a reagent in organic synthesis.
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| Names | |
|---|---|
| Preferred IUPAC name Heptanedioyl dichloride | |
| Identifiers | |
| 3D model (JSmol) | |
| ChemSpider | |
| ECHA InfoCard | 100.005.056 | 
| EC Number | 
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| PubChem CID | |
| UNII | |
| CompTox Dashboard (EPA) | |
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| Properties | |
| C7H10Cl2O2 | |
| Molar mass | 197.06 g·mol−1 | 
| Hazards | |
| GHS labelling: | |
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| Danger | |
| H315, H318, H335 | |
| P260, P261, P264, P271, P280, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P312, P321, P363, P403+P233, P405, P501 | |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references | |
Synthesis
    
Pimeloyl chloride can be synthesized from pimelic acid in thionyl chloride.[1]
References
    
- US 2014256775, CHEN LIN [US]; CHEN XIAOJIANG [US]; WU YONGQING[US]; GAI DAHAI [US], "NOVEL TRANSCRIPTION FACTOR MODULATORS"
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