CAS 2014-75-7
:2-(Phenylthio)ethanamine
Description:
2-(Phenylthio)ethanamine, also known as phenylthioethylamine, is an organic compound characterized by the presence of both an amine and a thioether functional group. Its molecular structure features a two-carbon ethyl chain attached to a phenylthio group (–SPh) and an amino group (–NH2). This compound typically appears as a colorless to pale yellow liquid or solid, depending on its purity and form. It is soluble in organic solvents and exhibits moderate polarity due to the presence of the amino group. The compound is of interest in various fields, including medicinal chemistry, where it may serve as a precursor for synthesizing other biologically active molecules. Its reactivity is influenced by the amino group, which can participate in nucleophilic substitution reactions, while the phenylthio group can enhance lipophilicity and influence the compound's biological activity. Safety precautions should be taken when handling this substance, as it may pose health risks if ingested or inhaled.
Formula:C8H12NS
InChI:InChI=1/C8H11NS/c9-6-7-10-8-4-2-1-3-5-8/h1-5H,6-7,9H2/p+1
Synonyms:- 2-(Phenylsulfanyl)Ethanamine
- 2-(Phenylsulfanyl)Ethanaminium
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Found 3 products.
2-(Phenylsulfanyl)ethan-1-amine
CAS:2-(Phenylsulfanyl)ethan-1-amineFormula:C8H11NSPurity:techColor and Shape: colourless to yellow liquidMolecular weight:153.24g/mol2-(Phenylthio)ethanamine hydrochloride
CAS:<p>2-Phenylthioethanamine hydrochloride is a synthetic, water soluble and lipophilic compound with a molecular weight of 171.2 g/mol. It is an antagonist of the -receptor and binds to the transporter protein. This drug is used for diagnostic purposes in angiography, phthalate determination, stable complexes for diagnosis and polymerase chain reaction (PCR) enzyme activities. 2-Phenylthioethanamine hydrochloride has been found to inhibit tumor growth in mice treated with radiation or chemotherapy. It has also been shown to be effective in the treatment of popliteal tumors in rats. The drug has been shown to be effective against bacteria that are resistant to antibiotics such as methicillin and amoxicillin. This drug also has effects on clinical relevance by inhibiting enzymes involved in clinical relevance such as acetylcholinesterase, phosphodiesterase and lipases.</p>Formula:C8H11NSPurity:Min. 95%Color and Shape:PowderMolecular weight:153.25 g/mol


