Ethoxyethyne

Ethoxyethyne
  • CAS No.:927-80-0
Other grades of this product :
Ethoxyethyne Basic information
Product Name:Ethoxyethyne
Synonyms:Ethoxyacetylene,ca50%w/winhexanes;ETHYL ETHYNYL ETHER,50wt% SOLUITON IN HEXANES;Ethoxyacetylene, 50% hexane solution;ETHOXYACETYLENE(40% W/W SOLUTION IN HEXANES);ETHYL ETHYNYL ETHER: (50% BY WT. IN HEXANE);Ethynyl ethyl ether;Ethyl ethynyl ether, 40 WT% solution in hexanes;ETHYL ETHYNYL ETHER, 50% (W/W) In HEXANES
CAS:927-80-0
MF:C4H6O
MW:70.09
EINECS:213-164-5
Product Categories:Alkynes;Organic Building Blocks;Terminal
Mol File:927-80-0.mol
Ethoxyethyne Chemical Properties
Boiling point 53°C
density 0.732 g/mL at 25 °C
refractive index n20/D 1.379
Fp −20 °F
storage temp. 2-8°C
Water Solubility Slightly miscible with water.
BRN 741882
Exposure limitsACGIH: TWA 50 ppm (Skin)OSHA: TWA 500 ppm(1800 mg/m3)NIOSH: IDLH 1100 ppm; TWA 50 ppm(180 mg/m3)
CAS DataBase Reference927-80-0(CAS DataBase Reference)
NIST Chemistry ReferenceEthoxyacetylene(927-80-0)
Safety Information
Hazard Codes F,Xn,N
Risk Statements 11-38-48/20-51/53-62-65-67-36/37/38-36/38
Safety Statements 16-36/37-61-62-45-36/37/39-26-33-29-9
RIDADR UN 1993 3/PG 2
WGK Germany 3
RTECS KN9900000
Hazard Note Highly Flammable/Keep Cold
HazardClass 3
PackingGroup II
HS Code 29091990
MSDS Information
ProviderLanguage
Ethyl ethynyl ether English
SigmaAldrich English
ACROS English
ALFA English
Ethoxyethyne Usage And Synthesis
Chemical PropertiesClear orange to brown solution
UsesEthoxyacetylene is used in Arens-van Dorp synthesis to prepare propargyl alcohol via reaction with ketone. In organic synthesis, it undergoes [2+2] cycloaddition reactions with ketenes to give cyclobutenone derivatives. It is also used to prepare alpha, beta-unsaturated esters from ketones by following Meyer-Schuster rearrangement.Used with N-vinylamides and triflic anhydride in a direct, three-component synthesis of pyridines. Also used to prepare α, β-unsaturated esters from ketones via a Meyer-Schuster rearrangement.
UsesUsed with N-vinylamides and triflic anhydride in a direct, three-component synthesis of pyridines. Also used to prepare α,β-unsaturated esters from ketones via a Meyer-Schuster rearrangement.

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