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Thermo Scientific Chemicals
Methyl 3-aminothiophene-2-carboxylate, 98+%
CAS: 22288-78-4 | C6H7NO2S | 157.19 g/mol
化学物質識別子
CAS22288-78-4
IUPAC Namemethyl 3-aminothiophene-2-carboxylate
Molecular FormulaC6H7NO2S
InChI KeyTWEQNZZOOFKOER-UHFFFAOYSA-N
SMILESCOC(=O)C1=C(N)C=CS1
さらに表示
仕様
スペックシート
スペックシートAssay (Non-aqueous acid-base Titration)≥98.0 to ≤102.0%
FormCrystals or powder or crystalline powder
Appearance (Color)Cream to pale brown
Melting Point (clear melt)63.0-69.0?C
Methyl 3-aminothiophene-2-carboxylate is used in the synthesis of 4-nitro and 4-aminothienyl ureas, total synthesis of quinazolinocarboline alkaloids and in preparation of thienopyrimidinone analogs.
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
Methyl 3-aminothiophene-2-carboxylate is used in the synthesis of 4-nitro and 4-aminothienyl ureas, total synthesis of quinazolinocarboline alkaloids and in preparation of thienopyrimidinone analogs.
Solubility
Slightly soluble in water.
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place.
Methyl 3-aminothiophene-2-carboxylate is used in the synthesis of 4-nitro and 4-aminothienyl ureas, total synthesis of quinazolinocarboline alkaloids and in preparation of thienopyrimidinone analogs.
Solubility
Slightly soluble in water.
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place.
RUO – Research Use Only
General References:
- John M. Barkera.; Patrick R. Huddlestona.; Michael L. An Easy Synthesis of 3-Amino- and 3-Nitrothiophene. Synthetic Communications: An International Journal for Rapid Communication of Synthetic Organic Chemistry. 1995, 25 (23), 3729-3734.
- Wu Yun Ren.; Mu Ill Lim.; Brian A. Otter.; Robert S. Klein. Synthetic studies of the thieno[3,2-d]pyrimidine C-nucleoside isostere of inosine. J. Org. Chem. 1982, 47 (24), 4633-4637.