2-methoxythiophene

2-methoxythiophene

3-bromo-2-iodo-thiophene

3-bromo-2-iodo-thiophene

methyl4-aminothiophene-3-carboxylate

$250.00
CAS No.: 69363-85-5
Catalog No.: 194493
Purity: 95%
MF: C6H7NO2S
MW: 157.194
Storage: 2-8 degree Celsius
SMILES: COC(=O)C1=CSC=C1N
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194493
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methyl4-aminothiophene-3-carboxylate; CAS No.: 69363-85-5; methyl4-aminothiophene-3-carboxylate. PROPERTIES: methyl4-aminothiophene-3-carboxylate is a crystalline solid. Its molecular formula is C6H7NOS2, and the molecular weight is approximately 185.26 g/mol. The compound has a melting point of approximately 100-102 C. It is slightly soluble in water but dissolves well in organic solvents such as methanol and dimethylformamide. For proper storage, it should be kept in a sealed container at room temperature, away from heat and direct sunlight. As a compound containing a thiophene ring, an amino group, and an ester group, it may exhibit certain reactivity and stability. When handling it, protective gloves and eye protection should be worn. In case of accidental contact with skin or eyes, immediate rinsing with water is necessary. APPLICATIONS: In organic synthesis, methyl4-aminothiophene-3-carboxylate serves as a versatile intermediate. The amino group can undergo various reactions such as acylation, sulfonation, and diazotization. The ester group can be hydrolyzed to a carboxylic acid. In the pharmaceutical industry, derivatives of this compound can be explored as potential drug candidates. For example, in the development of certain anti-inflammatory drugs, the structure of methyl4-aminothiophene-3-carboxylate can be modified to enhance the drug's efficacy and reduce side effects (as described in medicinal chemistry research articles). Additionally, in the field of chemical research, it can be used as a starting material for the synthesis of novel organic compounds with potential applications in catalysis and sensing (as mentioned in organic chemistry research papers).

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