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1-ACETOXY-1-CYANOETHYLENE

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1-ACETOXY-1-CYANOETHYLENE Basic information

Product Name:
1-ACETOXY-1-CYANOETHYLENE
Synonyms:
  • 1-Cyanovinyl ester of acetic acid
  • 1-Kyanvinylester kyseliny octove
  • 1-kyanvinylesterkyselinyoctove
  • 2-(acetyloxy)-2-propenenitril
  • 2-(acetyloxy)-2-propenenitrile
  • 2-hydroxy-acrylonitrilacetate
  • 2-hydroxy-acrylonitrilacetate(ester)
  • 2-Hydroxyacrylonitrile acetate
CAS:
3061-65-2
MF:
C5H5NO2
MW:
111.1
EINECS:
221-303-6
Product Categories:
  • Nitrogen Compounds
  • Organic Building Blocks
  • Building Blocks
  • C1 to C5
  • Chemical Synthesis
  • Cyanides/Nitriles
Mol File:
3061-65-2.mol
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1-ACETOXY-1-CYANOETHYLENE Chemical Properties

Boiling point:
80-82 °C30 mm Hg(lit.)
Density 
1.061 g/mL at 20 °C(lit.)
vapor pressure 
30 mm Hg ( 80 °C)
refractive index 
n20/D 1.426(lit.)
Flash point:
147 °F
storage temp. 
Sealed in dry,2-8°C
solubility 
sol most organic solvents other than pure hydrocarbons.
form 
clear liquid
color 
Colorless to Light yellow
BRN 
1751158
CAS DataBase Reference
3061-65-2(CAS DataBase Reference)
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Safety Information

Hazard Codes 
T
Risk Statements 
23/24/25-41-37/38
Safety Statements 
36/37/39-45-26
RIDADR 
UN 3276 6.1/PG 2
WGK Germany 
3
RTECS 
AG4550000
HS Code 
2926.90.5050
HazardClass 
6.1(a)
PackingGroup 
II
Toxicity
skn-rbt 10 mg/24H open MLD AIHAAP 23,95,62

MSDS

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1-ACETOXY-1-CYANOETHYLENE Usage And Synthesis

Reactivity Profile

1-cyanovinyl acetate is a ketene equivalent for use in the Diels-Alder reaction; undergoes other cycloaddition reactions; reacts with nucleophiles and radicals[1].

Safety Profile

Poison by inhalation, ingestion, andskin contact. A skin irritant. Whenheated to decomposition it emits toxic fumes of NOx andCN-.

storage

Handling, Storage, and Precautions: highly toxic; use only in a fume hood. Reagent can be absorbed through the skin. Always wear gloves when handling this reagent.

References

1. Ranganathan, S.; Ranganathan, D.; Mehrotra, A. K. S 1977, 289.
2. Brown, D. S.; Paquette, L. A. JOC 1992, 57, 4512.
3. Nowak, R. M. JOC 1963, 28, 1182.

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