Pimeloyl chloride
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Names | |
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Preferred IUPAC name
Heptanedioyl dichloride | |
Identifiers | |
3D model (JSmol) |
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ChemSpider | |
EC Number | 205-561-7 |
PubChem CID |
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Properties | |
C7H10Cl2O2 | |
Molar mass | 197.06 g·mol−1 |
Hazards | |
GHS pictograms | ![]() ![]() |
GHS signal word | Danger |
H315, H318, H335 | |
P260, P261, P264, P271, P280, P301+330+331, P303+361+353, P304+340, P305+351+338, P310, P312, P321, P363, P403+233, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
Pimeloyl chloride is a di-acyl chloride. It is used as a reagent in organic synthesis.
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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