Atomfair tert-butyl N-(4-hydroxy-3-methylphenyl)carbamate C12H17NO3

Description tert-butyl N-(4-hydroxy-3-methylphenyl)carbamate (CAS No. 218966-28-0) is a high-purity carbamate derivative widely used in pharmaceutical and organic synthesis research. With the molecular formula C12H17NO3, this compound serves as a versatile building block for the development of bioactive molecules. Its IUPAC name, tert-butyl N-(4-hydroxy-3-methylphenyl)carbamate , reflects its structural features, including a tert-butoxycarbonyl (Boc) protecting group and a phenolic hydroxyl moiety, making it ideal for selective deprotection and further functionalization. This product is rigorously tested for quality, ensuring optimal performance in sensitive applications. Available in various quantities, it is packaged under inert conditions to guarantee stability and longevity.

Description

tert-butyl N-(4-hydroxy-3-methylphenyl)carbamate (CAS No. 218966-28-0) is a high-purity carbamate derivative widely used in pharmaceutical and organic synthesis research. With the molecular formula C₁₂H₁₇NO₃, this compound serves as a versatile building block for the development of bioactive molecules. Its IUPAC name, tert-butyl N-(4-hydroxy-3-methylphenyl)carbamate, reflects its structural features, including a tert-butoxycarbonyl (Boc) protecting group and a phenolic hydroxyl moiety, making it ideal for selective deprotection and further functionalization. This product is rigorously tested for quality, ensuring optimal performance in sensitive applications. Available in various quantities, it is packaged under inert conditions to guarantee stability and longevity.

CAS No: 218966-28-0
Molecular Formula: C12H17NO3
Molecular Weight: 223.27
Exact Mass: 223.12084340
Monoisotopic Mass: 223.12084340
IUPAC Name: tert-butyl N-(4-hydroxy-3-methylphenyl)carbamate
SMILES: CC1=C(C=CC(=C1)NC(=O)OC(C)(C)C)O
Synonyms: 218966-28-0, tert-butyl N-(4-hydroxy-3-methylphenyl)carbamate, 958-739-8, 4-(Boc-amino)-2-methylphenol, MFCD24126282

Application

tert-butyl N-(4-hydroxy-3-methylphenyl)carbamate is primarily employed as an intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other therapeutic agents. Its Boc-protected amine group allows for selective deprotection under mild acidic conditions, facilitating stepwise organic synthesis. Researchers also utilize this compound in peptide coupling reactions and as a precursor for advanced material science applications. Its stability and reactivity make it a valuable tool for medicinal chemistry and drug discovery workflows.

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