4-(pyrrolidin-1-yl)aniline

4-(pyrrolidin-1-yl)aniline

2,5-dioxopyrrolidin-1-yl 7-methoxy-2-oxo-2H-chromene-3-carboxylate

2,5-dioxopyrrolidin-1-yl 7-methoxy-2-oxo-2H-chromene-3-carboxylate

2,5-dioxopyrrolidin-1-yl 3-mercaptopropanoate

$200.00
CAS No.: 117235-10-6
Catalog No.: 194850
Purity: 95%
MF: C7H9NO4S
MW: 203.219
Storage: 2-8 degree Celsius
SMILES: O=C(ON1C(CCC1=O)=O)CCS
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194850
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2,5-dioxopyrrolidin-1-yl 3-mercaptopropanoate; CAS No.: 117235-10-6; 2,5-dioxopyrrolidin-1-yl 3-mercaptopropanoate. PROPERTIES: 2,5-dioxopyrrolidin-1-yl 3-mercaptopropanoate is a crystalline solid. Its molecular formula is C7H10N2O3S, and the molecular weight is approximately 214.23 g/mol. The compound has a melting point of approximately 70-72 C. It is moderately soluble in common organic solvents such as methanol and dimethylformamide, but is poorly soluble in water. 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 pyrrolidinedione ring and a mercapto 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, 2,5-dioxopyrrolidin-1-yl 3-mercaptopropanoate serves as a versatile intermediate. The mercapto group can undergo various reactions such as oxidation and alkylation. The pyrrolidinedione ring provides opportunities for further functionalization. In the pharmaceutical industry, derivatives of this compound can be explored as potential drug candidates. For example, in the development of certain antimicrobial agents, the structure of 2,5-dioxopyrrolidin-1-yl 3-mercaptopropanoate can be modified to enhance the drug's antimicrobial activity and selectivity (as reported in medicinal chemistry journals). 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 noted in organic chemistry research papers).

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