ChemicalBook Product Catalog Pharmaceutical intermediates Heterocyclic compound Thiophene compounds 2-Thiopheneacetonitrile

2-Thiopheneacetonitrile

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
2-Thiopheneacetonitrile Structure
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.)
Fp 215 °F
storage temp. Keep in dark place,Inert atmosphere,Room temperature
form clear liquid
Specific Gravity1.157
color Colorless to Light orange to Yellow
BRN 106960
CAS DataBase Reference20893-30-5(CAS DataBase Reference)
NIST Chemistry Reference2-Thiopheneacetonitrile(20893-30-5)
EPA Substance Registry System2-Thiopheneacetonitrile (20893-30-5)
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 Information
ProviderLanguage
Thien-2-ylacetonitrile English
SigmaAldrich English
ACROS English
ALFA English
2-Thiopheneacetonitrile Usage And Synthesis
Chemical Propertiesclear colourless to slightly brown liquid
Uses2-Thiopheneacetonitrile was used as reagent during the synthesis of monodisperse Au/Au@polythiophene core/shell nanospheres.
DefinitionChEBI: 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
2,3-thiopheneacetonitrile,3-THIOPHENEACETONITRILE 2-[3-CHLORO-5-(TRIFLUOROMETHYL)-2-PYRIDINYL]-2-(2-THIENYL)ACETONITRILE acetonitrile 3-(4-METHOXYANILINO)-2-(2-THIENYL)ACRYLONITRILE 2-(2-THIENYL)-3-(4-TOLUIDINO)ACRYLONITRILE 2-Thiopheneacetonitrile METHYL 3-AMINO-1-CYANO-4-FLUORO-1-(2-THIENYL)-1H-INDENE-2-CARBOXYLATE 2-[5-(2-FLUOROBENZOYL)-2-THIENYL]ACETONITRILE 2-(5-BENZOYL-2-THIENYL)ACETONITRILE 2-[5-(4-METHOXYBENZOYL)-2-THIENYL]ACETONITRILE 2-Thiopheneacetic acid (E)-3-(1,3-BENZODIOXOL-5-YL)-2-(2-THIENYL)-2-PROPENENITRILE 2-[5-(4-CHLOROBENZOYL)-2-THIENYL]ACETONITRILE Iminodiacetonitrile 3-AMINO-4-FLUORO-1-(2-THIENYL)-1H-INDENE-1,2-DICARBONITRILE 2-[3-CHLORO-5-(TRIFLUOROMETHYL)-2-PYRIDINYL]-2-MORPHOLINO-2-(2-THIENYL)ACETONITRILE Tetrahydrothiophene 2-[CYANO(2-THIENYL)METHYL]-6-FLUOROBENZENECARBONITRILE
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