Hexanoyl chloride

Hexanoyl chloride
Names
Other names
Caproyl chloride
Identifiers
3D model (JSmol)
ChemSpider
EC Number 205-549-1
UNII
Properties
C6H11ClO
Molar mass 134.60 g·mol−1
Hazards
GHS pictograms
GHS signal word Danger
H226, H302, H314, H335
P210, P233, P240, P241, P242, P243, P260, P261, P264, P270, P271, P280, P301+312, P301+330+331, P303+361+353, P304+340, P305+351+338, P310, P312, P321, P330, P363, P370+378, P403+233, P403+235
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

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

  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.
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