| Identification | Back Directory | [Name]
N,N-diethylthiophene-3-carboxylamide | [CAS]
73540-75-7 | [Synonyms]
N,N-diethyl-3-Thiophenecarboxamide
N,N-diethylthiophene-3-carboxylamide
3-ThiophenecarboxaMide, N,N-diethyl-
3-thiophenecarboxylic acid,N,N-diethylamide | [Molecular Formula]
C9H13NOS | [MDL Number]
MFCD11742083 | [MOL File]
73540-75-7.mol | [Molecular Weight]
183.27 |
| Chemical Properties | Back Directory | [Boiling point ]
296.0±13.0 °C(Predicted) | [density ]
1.096±0.06 g/cm3(Predicted) | [storage temp. ]
Keep in dark place,Sealed in dry,2-8°C | [pka]
-0.85±0.70(Predicted) | [InChI]
InChI=1S/C9H13NOS/c1-3-10(4-2)9(11)8-5-6-12-7-8/h5-7H,3-4H2,1-2H3 | [InChIKey]
DMGZZYONMSPHOF-UHFFFAOYSA-N | [SMILES]
C1SC=CC=1C(N(CC)CC)=O |
| Hazard Information | Back Directory | [Synthesis]
Diethylamine (60 mL) was added to a 500 mL round bottom flask and cooled in an ice bath. Thiophene-3-carbonyl chloride (compound g-1) was dissolved in 10 mL of dichloromethane and slowly added dropwise to the reaction flask. The reaction mixture was stirred at room temperature for 30 minutes. Subsequently, the organic phase was separated by extraction with dichloromethane and NaCl aqueous solution to afford dark yellow liquid N,N-diethyl-3-thiophenecarboxamide (compound g-2) in 58% yield. | [References]
[1] Journal of Materials Chemistry A, 2016, vol. 4, # 47, p. 18409 - 18415
[2] Tetrahedron, 2016, vol. 72, # 17, p. 2219 - 2225
[3] Macromolecules, 2014, vol. 47, # 3, p. 1008 - 1020
[4] New Journal of Chemistry, 2015, vol. 39, # 3, p. 2248 - 2255
[5] Patent: KR101495152, 2015, B1. Location in patent: Paragraph 0184; 0188-0189 |
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Struchem Co., Ltd.
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0512-63009836 18994340901 |
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Grader reagent
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