Pimeloyl chloride

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Pimeloyl chloride
Pimeloyl chloride.svg
Names
Preferred IUPAC name
Heptanedioyl dichloride
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.005.056 Edit this at Wikidata
EC Number
  • 205-561-7
UNII
  • InChI=1S/C7H10Cl2O2/c8-6(10)4-2-1-3-5-7(9)11/h1-5H2
    Key: LVIMBOHJGMDKEJ-UHFFFAOYSA-N
  • C(CCC(=O)Cl)CCC(=O)Cl
Properties
C7H10Cl2O2
Molar mass 197.06 g·mol−1
Hazards
GHS labelling:
GHS05: CorrosiveGHS07: Exclamation mark
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]

  1. ^ US 2014256775, CHEN LIN [US]; CHEN XIAOJIANG [US]; WU YONGQING[US]; GAI DAHAI [US], "NOVEL TRANSCRIPTION FACTOR MODULATORS"