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Hexanoyl chloride

From Wikipedia, the free encyclopedia
Hexanoyl chloride
Names
Preferred IUPAC name
Hexanoyl chloride
Other names
Caproyl chloride
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.005.045 Edit this at Wikidata
EC Number
  • 205-549-1
UNII
  • InChI=1S/C6H11ClO/c1-2-3-4-5-6(7)8/h2-5H2,1H3
    Key: YWGHUJQYGPDNKT-UHFFFAOYSA-N
  • CCCCCC(=O)Cl
Properties
C6H11ClO
Molar mass 134.60 g·mol−1
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
Maybe toxic and corrosive
GHS labelling:
GHS02: FlammableGHS05: CorrosiveGHS07: Exclamation mark
Danger
H226, H302, H314, H335
P210, P233, P240, P241, P242, P243, P260, P261, P264, P270, P271, P280, P301+P312, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P312, P321, P330, P363, P370+P378, P403+P233, P403+P235, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Hexanoyl chloride is a six-carbon acyl chloride with a straight-chain structure that is used as a reagent in organic synthesis.[1][2][3][4]

References

[edit]
  1. ^ "Hexanoyl chloride". Sigma-Aldrich. Retrieved 1 July 2017.
  2. ^ Jeremy P. E. Spencer; Alan Crozier (24 April 2012). Flavonoids and Related Compounds: Bioavailability and Function. CRC Press. pp. 263–4. ISBN 978-1-4398-4827-2.
  3. ^ Vijay Kumar Thakur; Amar Singh Singha (27 April 2015). Surface Modification of Biopolymers. John Wiley & Sons. p. 265. ISBN 978-1-118-66955-6.
  4. ^ Robert Martin; Jean-Pierre Buisson (24 February 2015). Aromatic Hydroxyketones: Preparation & Physical Properties: Aromatic Hydroxyketones from Butanone (C4) to Dotriacontanone (C32). Springer. pp. 661 etc. ISBN 978-3-319-14185-5.