CAS 5285-74-5

Thiocyanic acid, 4-methylphenyl ester

Description:

Thiocyanic acid, 4-methylphenyl ester, also known as 4-methylphenyl thiocyanate, is an organic compound characterized by the presence of a thiocyanate functional group (-SCN) attached to a 4-methylphenyl group. This compound typically appears as a colorless to pale yellow liquid with a distinctive odor. It is soluble in organic solvents but has limited solubility in water due to its hydrophobic aromatic structure. The compound is known for its reactivity, particularly in nucleophilic substitution reactions, and can serve as a precursor in the synthesis of various organic compounds. Its applications may extend to the fields of pharmaceuticals, agrochemicals, and materials science. Safety considerations are important when handling this compound, as it may pose health risks if inhaled or ingested, and appropriate precautions should be taken to minimize exposure. Overall, thiocyanic acid, 4-methylphenyl ester is a notable compound in organic chemistry with diverse potential applications.

Formula: C₈H₇NS

[(4-Methylphenyl)sulfanyl]formonitrile

CAS: 5285-74-5

[(4-Methylphenyl)sulfanyl]formonitrile is a reactive chemical that is used in the synthesis of organic and organometallic compounds. It has been shown to be an effective thiocyanation agent, which may be due to its ability to form cyanate upon reaction with sulfide. The cross-coupling mechanism for [(4-Methylphenyl)sulfanyl]formonitrile is not well understood, but it does not appear to involve the formation of sulfur transfer or a mechanistic intermediate. This reactive compound has two functional groups that are similar to those found in biomolecules such as amino acids and nucleic acids.

Formula: C₈H₇NS

Purity: Min. 95%

Molecular weight: 149.21 g/mol

Ref: 3D-FAA28574