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Atomfair Tert-butyl m-tolylcarbamate C12H17NO2

Description Tert-butyl m-tolylcarbamate (CAS No. 18437-67-7) is a high-purity carbamate derivative with the molecular formula C12H17NO2. This compound, also known as tert-butyl N-(3-methylphenyl)carbamate , is a valuable intermediate in organic synthesis and pharmaceutical research. Its structural features include a tert-butyl carbamate group attached to a meta-substituted toluene ring, offering versatility in chemical modifications. Ideal for researchers, this product is rigorously tested for purity and stability, ensuring reliable performance in synthetic applications. Available in various quantities, it is supplied with comprehensive analytical data (including HPLC, NMR, and MS) to meet stringent laboratory standards.

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Description

Description

Tert-butyl m-tolylcarbamate (CAS No. 18437-67-7) is a high-purity carbamate derivative with the molecular formula C12H17NO2. This compound, also known as tert-butyl N-(3-methylphenyl)carbamate, is a valuable intermediate in organic synthesis and pharmaceutical research. Its structural features include a tert-butyl carbamate group attached to a meta-substituted toluene ring, offering versatility in chemical modifications. Ideal for researchers, this product is rigorously tested for purity and stability, ensuring reliable performance in synthetic applications. Available in various quantities, it is supplied with comprehensive analytical data (including HPLC, NMR, and MS) to meet stringent laboratory standards.

  • CAS No: 18437-67-7
  • Molecular Formula: C12H17NO2
  • Molecular Weight: 207.27
  • Exact Mass: 207.125928785
  • Monoisotopic Mass: 207.125928785
  • IUPAC Name: tert-butyl N-(3-methylphenyl)carbamate
  • SMILES: CC1=CC(=CC=C1)NC(=O)OC(C)(C)C
  • Synonyms: tert-butyl m-tolylcarbamate, 18437-67-7, tert-butyl N-(3-methylphenyl)carbamate, tert-Butylm-tolylcarbamate, MFCD07127701

Application

Tert-butyl m-tolylcarbamate serves as a key building block in the synthesis of pharmaceuticals, agrochemicals, and specialty materials. Its carbamate moiety is useful for protecting amine groups during multi-step reactions. Researchers also employ it in the development of enzyme inhibitors and polymer precursors. The meta-tolyl group enhances solubility and reactivity in organic transformations.

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