dimethyl 4-amino-2,3-thiophenedicarboxylate

dimethyl 4-amino-2,3-thiophenedicarboxylate - Names and Identifiers

Name	dimethyl 4-aminothiophene-2,3-dicarboxylate
Synonyms	AKOS 221-05 BUTTPARK 15418-53 METHYL 4-AMINOTHIOPHENE-2,3-DICARBOXYLATE Dimethyl 4-aminothiophene-2,3-dicarboxylate dimethyl 4-aminothiophene-2,3-dicarboxylate dimethyl 4-amino-2,3-thiophenedicarboxylate DIMETHYL 4-AMINOTHIOPHENE-2,3-DICARBOXYLATE 2,3-diMethyl 4-aMinothiophene-2,3-dicarboxylate 4-amino-2-methoxycarbonyl-3-thiophenecarboxylate 4-Amino-thiophene-2,3-dicarboxylic acid dimethyl ester
CAS	62947-31-3

dimethyl 4-amino-2,3-thiophenedicarboxylate - Physico-chemical Properties

Molecular Formula	C8H9NO4S
Molar Mass	215.23
Storage Condition	2-8°C

dimethyl 4-amino-2,3-thiophenedicarboxylate - Risk and Safety

Hazard Symbols	Xi - Irritant
Hazard Note	Irritant

dimethyl 4-amino-2,3-thiophenedicarboxylate - Introduction

dimethyl 4-aminothiophene-2,3-dicarboxylate is an organic compound with the chemical formula C8H9NO4S. It is a white crystalline solid with a special smell.

The compound has some important properties. First, it has a high melting point and boiling point, and is stable at room temperature. It is soluble in organic solvents, but insoluble in water. It is a moderately strong acidic substance that can react with bases to form salts. In addition, dimethyl 4-aminothiophene-2,3-dicarboxylate is also an organic fluorescent substance and has a light-emitting property.

dimethyl 4-aminothiophene-2,3-dicarboxylate has a wide range of uses in chemical research and industrial production. It can be used as an intermediate of optical materials for the synthesis of fluorescent dyes and fluorescent labeling reagents. In addition, it can also be used as a raw material for electrochemical materials to prepare batteries and current sensors with special properties.

The method for preparing dimethyl 4-aminothiophene-2,3-dicarboxylate is generally obtained by reacting a dihalo derivative of thiophene with formic anhydride. Specifically, the dibromo derivative of thiophene can be first reacted with formic anhydride to form dimethyl dicarboxylate of thiophene, and then reacted with the corresponding amine to obtain the final dimethyl 4-aminothiophene-2,3-dicarboxylate.

For safety information, dimethyl 4-aminothiophene-2,3-dicarboxylate is a relatively safe compound under routine conditions. However, it is still a chemical, and the corresponding experimental operation and safety measures should be followed when using it, and it should be stored properly. During the operation, direct contact with skin, eyes and respiratory tract should be avoided. When handling or storing, it is necessary to maintain proper ventilation and keep it away from ignition and flammable materials. If ingested or in contact with skin or eyes, rinse immediately with plenty of water and seek medical advice.

Last Update：2024-04-10 22:29:15