1-Decyne

Source: Wikipedia, the free encyclopedia.
1-Decyne
1-Decyne.svg
Names
Preferred IUPAC name
Dec-1-yne
Other names
1-Decyne
Identifiers
3D model (
JSmol
)
ChEBI
ChemSpider
ECHA InfoCard
100.011.029 Edit this at Wikidata
EC Number
  • 212-132-8
UNII
  • InChI=1S/C10H18/c1-3-5-7-9-10-8-6-4-2/h1H,4-10H2,2H3
    Key: ILLHQJIJCRNRCJ-UHFFFAOYSA-N
  • InChI=1/C10H18/c1-3-5-7-9-10-8-6-4-2/h1H,4-10H2,2H3
    Key: ILLHQJIJCRNRCJ-UHFFFAOYAE
  • C(#C)CCCCCCCC
Properties
C10H18
Molar mass 138.254 g·mol−1
Appearance Colorless liquid
Density 0.767 g/cm3
Melting point −44 °C (−47 °F; 229 K)
Boiling point 174 °C (345 °F; 447 K)
1.426–1.428
Hazards
GHS labelling:
GHS09: Environmental hazard
Danger
H226, H315, H318, H335, H410
P210, P233, P240, P241, P242, P243, P261, P264, P271, P273, P280, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P310, P312, P321, P332+P313, P362, P370+P378, P391, P403+P233, P403+P235, P405, P501
Flash point 48 °C (118 °F; 321 K)
Safety data sheet (SDS) External MSDS
Related compounds
Related Alkynes
Octyne
Nonyne
Undecyne
Dodecyne
Related compounds
Decanol
Decene
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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1-Decyne is the

Huisgen cycloadditions,[2] and borylations.[3]

Under the catalysis of platinum, it reacts with hydrogen to produce decane.[4]

See also

References

  1. PMID 16097019
    .
  2. .
  3. .
  4. ISSN 2046-2069. Retrieved 2021-11-16.{{cite journal}}: CS1 maint: multiple names: authors list (link
    )