Pimeloyl chloride
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Names | |
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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). |
Pimeloyl chloride is a di-acyl chloride. It is used as a reagent in organic synthesis.
Synthesis[edit]
Pimeloyl chloride can be synthesized from pimelic acid in thionyl chloride.[1]
References[edit]
- ^ US 2014256775, CHEN LIN [US]; CHEN XIAOJIANG [US]; WU YONGQING[US]; GAI DAHAI [US], "NOVEL TRANSCRIPTION FACTOR MODULATORS"