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2-Thiopheneacetonitrile

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2-Thiopheneacetonitrile Basic information

Product Name:
2-Thiopheneacetonitrile
Synonyms:
  • 2-Thiopheneacetonitrile, tech., 94%
  • 2-(2-Thienyl)acetonitrile
  • 2-Thiopheneacetonitrile,94%,tech.
  • 2-(Cyanomethyl)thiophene, 2-(Thien-2-yl)ethanenitrile
  • 2-Thiopheneacetonitrile,96%
  • Thiophene-2-acetonitrile for synthesis
  • THIOPHENE-2-ACETONITRILE
  • thien-2-ylacetonitrile
CAS:
20893-30-5
MF:
C6H5NS
MW:
123.18
EINECS:
244-104-6
Product Categories:
  • Thiophenes & Benzothiophenes
  • Aromatic Nitriles
  • Thiophenes & Benzothiophenes
  • Thiophene&Benzothiophene
  • Heterocyclic Compounds
  • Thiophens
  • Building Blocks
  • C4 to C6
  • Chemical Synthesis
  • Heterocyclic Building Blocks
  • Thiophenes
Mol File:
20893-30-5.mol
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2-Thiopheneacetonitrile Chemical Properties

Melting point:
50-51 °C
Boiling point:
115-120 °C/22 mmHg (lit.) 235-238 °C (lit.)
Density 
1.157 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.542(lit.)
Flash point:
215 °F
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
form 
clear liquid
color 
Colorless to Light orange to Yellow
Specific Gravity
1.157
BRN 
106960
CAS DataBase Reference
20893-30-5(CAS DataBase Reference)
NIST Chemistry Reference
2-Thiopheneacetonitrile(20893-30-5)
EPA Substance Registry System
2-Thiopheneacetonitrile (20893-30-5)
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Safety Information

Hazard Codes 
Xn,Xi,T
Risk Statements 
20/21/22-36/37/38
Safety Statements 
26-36/37-23-36
RIDADR 
UN 3276 6.1/PG 3
WGK Germany 
3
Hazard Note 
Irritant
TSCA 
T
HazardClass 
6.1
PackingGroup 
III
HS Code 
29349990

MSDS

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2-Thiopheneacetonitrile Usage And Synthesis

Chemical Properties

clear colourless to slightly brown liquid

Uses

2-Thiopheneacetonitrile was used as reagent during the synthesis of monodisperse Au/Au@polythiophene core/shell nanospheres.

Definition

ChEBI: 2-thienylacetonitrile is a nitrile that is acetonitrile where one of the methyl hydrogens is substituted by a 2-thienyl group. It is a nitrile and a member of thiophenes. It derives from an acetonitrile.

Synthesis Reference(s)

The Journal of Organic Chemistry, 15, p. 81, 1950 DOI: 10.1021/jo01147a014
Synthesis, p. 40, 1987 DOI: 10.1055/s-1987-27834

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