Jump to content

Pimeloyl chloride

From Wikipedia, the free encyclopedia
Pimeloyl chloride
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"