Hexanoyl chloride

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]

Hexanoyl chloride

Names
Other names Caproyl chloride
Identifiers
CAS Number	142-61-0
3D model (JSmol)	Interactive image
ChemSpider	60671
ECHA InfoCard	100.005.045
EC Number	205-549-1
PubChem CID	67340
UNII	I7GE8HG3B2
CompTox Dashboard (EPA)	DTXSID8059718
InChI InChI=1S/C6H11ClO/c1-2-3-4-5-6(7)8/h2-5H2,1H3 Key: YWGHUJQYGPDNKT-UHFFFAOYSA-N
SMILES CCCCCC(=O)Cl
Properties
Chemical formula	C6H11ClO
Molar mass	134.60 g·mol^−1
Hazards
GHS pictograms
GHS Signal word	Danger
GHS hazard statements	H226, H302, H314, H335
GHS precautionary statements	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

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.