Ethyl 2-aminothiophene-3-carboxylate, 97%, Thermo Scientific Chemicals
Element SearchElement SearchStructure SearchStructure Search
Thermo Scientific Chemicals
Ethyl 2-aminothiophene-3-carboxylate, 97%, Thermo Scientific Chemicals
Have Questions?
Change viewbuttonViewtableView
Quantity:
25 g
100 g
ChemDexTry the chem dexTM web app
Catalog number H61559.14
also known as H61559-14
Price (EUR)/ Each
110,70
Online exclusive
123.00 
Save 12,30 (10%)
-
Add to cart
Quantity:
25 g
Request bulk or custom format
Price (EUR)/ Each
110,70
Online exclusive
123.00 
Save 12,30 (10%)
Add to cart
Ethyl 2-aminothiophene-3-carboxylate, 97%, Thermo Scientific Chemicals
Catalog numberH61559.14
Price (EUR)/ Each
110,70
Online exclusive
123.00 
Save 12,30 (10%)
-
Add to cart
Chemical Identifiers
CAS31891-06-2
IUPAC Nameethyl 2-aminothiophene-3-carboxylate
Molecular FormulaC7H9NO2S
InChI KeyMKJQYFVTEPGXIE-UHFFFAOYSA-N
SMILESCCOC(=O)C1=C(N)SC=C1
View more
SpecificationsSpecification SheetSpecification Sheet
FormLow melt solid or viscous liquid
Assay (GC)≥96.5%
Appearance (Color)Black
Ethyl 2-aminothiophene-3-carboxylate is used as an organic chemical synthesis intermediate.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Ethyl 2-aminothiophene-3-carboxylate is used as an organic chemical synthesis intermediate.

Solubility
Slightly soluble in water.

Notes
Stable under recommended storage conditions. Incompatible with oxidizing agents.
RUO – Research Use Only

General References:

  1. A.Mobinikhaledi; M.Kalhor; L.Taheri. Synthesis of some novel methyl- and ethyl- 2-aminothiophene-3-carboxylate and related Schiff-Bases. Asian Journal of Chemistry. 2010, 22,(9), 7399-7404.
  2. Stephanie Hesse; Enrico Perspicace; Gilbert Kirsch. Microwave-assisted synthesis of 2-aminothiophene-3-carboxylic acid derivatives, 3H-thieno[2,3-d]pyrimidin-4-one and 4-chlorothieno[2,3-d]pyrimidine. Tetrahedron Letters. 2007, 48,(30), 5261-5264.