2-(((5-bromothiophen-2-yl)methyl)thio)ethan-1-amine
$300.00
CAS No.: 852916-58-6
Catalog No.: 194514
Purity: 95%
MF: C7H10BrNS2
MW: 252.202
Storage: 2-8 degree Celsius
SMILES: BrC1=CC=C(S1)CSCCN
Catalog No.: 194514
Purity: 95%
MF: C7H10BrNS2
MW: 252.202
Storage: 2-8 degree Celsius
SMILES: BrC1=CC=C(S1)CSCCN
2-(((5-bromothiophen-2-yl)methyl)thio)ethan-1-amine; CAS No.: 852916-58-6; 2-(((5-bromothiophen-2-yl)methyl)thio)ethan-1-amine. PROPERTIES: 2-(((5-bromothiophen-2-yl)methyl)thio)ethan-1-amine is a crystalline solid. Its molecular formula is C7H10BrNOS, and the molecular weight is approximately 253.13 g/mol. The compound has a melting point of approximately 50-52 C. It is moderately soluble in common organic solvents such as methanol and ethyl acetate, 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 thiophene ring, a bromo group, a thioether group, and an amine 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-bromothiophen-2-yl)methyl)thio)ethan-1-amine serves as a versatile intermediate. The amine group can undergo various reactions such as acylation, sulfonation, and diazotization. The thioether group can be converted to other functional groups such as sulfide or disulfide. 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-bromothiophen-2-yl)methyl)thio)ethan-1-amine 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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