Propargyl chloride

From Wikipedia, the free encyclopedia
(Redirected from Chloropropyne)
Jump to navigation Jump to search
Propargyl chloride[1]
File:Propargyl chloride.svg
File:Propargyl-chloride-Spartan-MP2-3D-balls.png
Names
Preferred IUPAC name
3-Chloroprop-1-yne
Other names
Propargyl chloride, 3-Chloropropyne, 1-Chloro-2-propyne, 2-Propynyl chloride, Gamma-Chloroallylene, UN 2345
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard Lua error in Module:Wikidata at line 880: attempt to index field 'wikibase' (a nil value). Lua error in Module:Wikidata at line 880: attempt to index field 'wikibase' (a nil value).Lua error in Module:EditAtWikidata at line 29: attempt to index field 'wikibase' (a nil value).
EC Number
  • 210-856-9
E number Lua error in Module:Wikidata at line 880: attempt to index field 'wikibase' (a nil value).
UNII
  • {{#property:P3117}}Lua error in Module:EditAtWikidata at line 29: attempt to index field 'wikibase' (a nil value).
  • InChI=1S/C3H3Cl/c1-2-3-4/h1H,3H2 checkY
    Key: LJZPPWWHKPGCHS-UHFFFAOYSA-N checkY
  • InChI=1/C3H3Cl/c1-2-3-4/h1H,3H2
    Key: LJZPPWWHKPGCHS-UHFFFAOYAR
  • C#CCCl
Properties
C3H3Cl
Molar mass 74.51 g·mol−1
Appearance colorless liquid
Density 1.0306 g/cm3
Melting point −78 °C (−108 °F; 195 K)
Boiling point 57 °C (135 °F; 330 K)
Insoluble
Hazards
GHS labelling:
GHS02: FlammableGHS05: CorrosiveGHS06: Toxic
Danger
H225, H301, H314, H330, H331, H335, H412
P210, P233, P240, P241, P242, P243, P260, P261, P264, P270, P271, P273, P280, P284, P301+P310, P301+P330+P331, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P310, P311, P312, P320, P321, P322, P330, P361, P363, P370+P378, P403+P233, P403+P235, P405, P501
NFPA 704 (fire diamond)

Error: Image is invalid or non-existent.

3
3
1
Flash point 18 °C (64 °F; 291 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Propargyl chloride is an organic compound with the formula HC2CH2Cl. It is a colorless liquid and a lacrymator.[2] It is an alkylating agent that is used in organic synthesis.[3]

See also

[edit | edit source]

References

[edit | edit source]
  1. ^ *Merck Index, 11th Edition, 7820
  2. ^ Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
  3. ^ Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
[edit | edit source]