Understanding the Properties and Synthesis of (3-Isothiocyanatophenyl)methanol
The chemical identity and behavior of a compound are fundamental to its successful application in research and industry. (3-Isothiocyanatophenyl)methanol, identified by CAS number 179549-74-7, is a molecule of significant interest due to its dual functionality and broad utility. Understanding its physical and chemical properties, as well as efficient synthesis routes, is crucial for chemists aiming to leverage its potential. NINGBO INNO PHARMCHEM CO.,LTD., a prominent chemical manufacturer in China, is committed to providing high-quality (3-Isothiocyanatophenyl)methanol and detailed information about its characteristics.
The chemical name for CAS 179549-74-7 is (3-Isothiocyanatophenyl)methanol, with the molecular formula C8H7NOS and a molecular weight of 165.21. The presence of both a primary alcohol (hydroxymethyl group) and an isothiocyanate group on the phenyl ring makes this compound a highly reactive and versatile synthon. The isothiocyanate group (-N=C=S) is an electrophilic center that readily undergoes addition reactions with nucleophiles, such as amines, alcohols, and thiols, forming stable thiourea, thiocarbamate, and dithiocarbamate derivatives, respectively. These reactions are fundamental in constructing complex organic molecules.
The benzylic alcohol functionality (-CH2OH) offers another site for chemical modification. It can be easily oxidized to the corresponding aldehyde or carboxylic acid, esterified with various acids, or converted into alkyl halides or ethers. This dual reactivity allows for diverse synthetic strategies, making (3-Isothiocyanatophenyl)methanol a valuable intermediate in multi-step synthesis, particularly in the pharmaceutical and fine chemical industries. Researchers seeking to buy (3-Isothiocyanatophenyl)methanol can rely on manufacturers like NINGBO INNO PHARMCHEM CO.,LTD. to provide consistent purity and detailed technical specifications, essential for reproducible and successful experimental outcomes.
The synthesis of (3-Isothiocyanatophenyl)methanol typically involves the conversion of a precursor amine to the isothiocyanate, often via reaction with thiophosgene or a similar reagent, while ensuring the preservation of the alcohol group. The precise control over reaction conditions is vital to achieve high yields and purity. As a dedicated supplier, NINGBO INNO PHARMCHEM CO.,LTD. invests in robust synthesis protocols and analytical testing to guarantee the quality of the product. Our commitment to excellence ensures that clients receive a reliable chemical building block for their critical research and manufacturing needs, solidifying our position as a trusted partner in the chemical supply chain.
The chemical name for CAS 179549-74-7 is (3-Isothiocyanatophenyl)methanol, with the molecular formula C8H7NOS and a molecular weight of 165.21. The presence of both a primary alcohol (hydroxymethyl group) and an isothiocyanate group on the phenyl ring makes this compound a highly reactive and versatile synthon. The isothiocyanate group (-N=C=S) is an electrophilic center that readily undergoes addition reactions with nucleophiles, such as amines, alcohols, and thiols, forming stable thiourea, thiocarbamate, and dithiocarbamate derivatives, respectively. These reactions are fundamental in constructing complex organic molecules.
The benzylic alcohol functionality (-CH2OH) offers another site for chemical modification. It can be easily oxidized to the corresponding aldehyde or carboxylic acid, esterified with various acids, or converted into alkyl halides or ethers. This dual reactivity allows for diverse synthetic strategies, making (3-Isothiocyanatophenyl)methanol a valuable intermediate in multi-step synthesis, particularly in the pharmaceutical and fine chemical industries. Researchers seeking to buy (3-Isothiocyanatophenyl)methanol can rely on manufacturers like NINGBO INNO PHARMCHEM CO.,LTD. to provide consistent purity and detailed technical specifications, essential for reproducible and successful experimental outcomes.
The synthesis of (3-Isothiocyanatophenyl)methanol typically involves the conversion of a precursor amine to the isothiocyanate, often via reaction with thiophosgene or a similar reagent, while ensuring the preservation of the alcohol group. The precise control over reaction conditions is vital to achieve high yields and purity. As a dedicated supplier, NINGBO INNO PHARMCHEM CO.,LTD. invests in robust synthesis protocols and analytical testing to guarantee the quality of the product. Our commitment to excellence ensures that clients receive a reliable chemical building block for their critical research and manufacturing needs, solidifying our position as a trusted partner in the chemical supply chain.
Perspectives & Insights
Logic Thinker AI
“invests in robust synthesis protocols and analytical testing to guarantee the quality of the product.”
Molecule Spark 2025
“Our commitment to excellence ensures that clients receive a reliable chemical building block for their critical research and manufacturing needs, solidifying our position as a trusted partner in the chemical supply chain.”
Alpha Pioneer 01
“The chemical identity and behavior of a compound are fundamental to its successful application in research and industry.”