Benzylthioacetonitrile, with the CAS number 17377-30-9, is an organic compound characterized by the presence of both a benzyl group and a thioacetonitrile functional group. It typically appears as a colorless to pale yellow liquid or solid, depending on its purity and specific conditions. The compound is known for its distinctive thiol and nitrile functionalities, which contribute to its reactivity and potential applications in organic synthesis and medicinal chemistry. Benzylthioacetonitrile can participate in various chemical reactions, including nucleophilic substitutions and cyclization processes, making it a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals. Its molecular structure includes a benzyl moiety, which enhances its lipophilicity, potentially influencing its biological activity and solubility in organic solvents. Safety data indicates that, like many thiol-containing compounds, it should be handled with care due to potential toxicity and irritant properties. Proper storage and handling protocols are essential to ensure safety in laboratory settings.

BENZYLTHIOACETONITRILE

17377-30-9: Benzylthioacetonitrile, with the CAS number 17377-30-9, is an organic compound characterized by the presence of both a benzyl group and a thioacetonitrile functional group. It typically appears as a colorless to pale yellow liquid or solid, depending on its purity and specific conditions. The compound is known for its distinctive thiol and nitrile functionalities, which contribute to its reactivity and potential applications in organic synthesis and medicinal chemistry. Benzylthioacetonitrile can participate in various chemical reactions, including nucleophilic substitutions and cyclization processes, making it a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals. Its molecular structure includes a benzyl moiety, which enhances its lipophilicity, potentially influencing its biological activity and solubility in organic solvents. Safety data indicates that, like many thiol-containing compounds, it should be handled with care due to potential toxicity and irritant properties. Proper storage and handling protocols are essential to ensure safety in laboratory settings.

2-(benzylsulfanyl)acetonitrile

<p>2-(Benzylsulfanyl)acetonitrile is an intermediate in the synthesis of a number of biologically active compounds, including ornithine and paraformaldehyde. It is also an intermediate in the synthesis of 2-methyl-2-nitrosopropane, which is used as a reagent to prepare nitrosobenzene. 2-(Benzylsulfanyl)acetonitrile can be reacted with various organic compounds to produce a variety of products. For example, when it reacts with paraformaldehyde, it yields 2-benzylthioacetonitrile and 2-hydroxyethyl methacrylate. When reacted with acetone, it yields methyl 3-(2-acetonylbenzylthio)-3-cyanopropionate. This product has been used as a synthase inhibitor in inflammation research and as an adrenergic receptor blocker for the treatment of asthma.</p>

CAS 17377-30-9

BENZYLTHIOACETONITRILE

2-(benzylsulfanyl)acetonitrile

Ref: IN-DA001Z6K

2-(Benzylsulfanyl)acetonitrile

Ref: 3D-SAA37730