9-Fluorenylmethyl N-hydroxycarbamate -

REF #: 3D-QHA65601
Short description

9-Fluorenylmethyl N-hydroxycarbamate: A Versatile Compound for Innovative Synthesis

Discover the exceptional 9-Fluorenylmethyl N-hydroxycarbamate, a labile compound with a remarkable purity of at least 95%. This unique chemical, bearing the CAS number 190656-01-0, is a stereoisomer of fluorenylmethyl carbamate, synthesized through the reaction of chloroformate and 9-fluorenone. Its molecular weight of 255.27 g/mol and formula of C15H13NO3 make it a valuable asset for advanced research and development.

Renowned for its effectiveness as an antibiotic against tuberculosis in mice, this compound offers a versatile platform for innovative synthesis. The synthesis process involves the activation of peptidyl chloride, which is then linked to hydroxamic acid or carboxylate, starting from solid phase and culminating in cellular biosynthesis. Unlock the potential of this exceptional chemical in your laboratory, where it can serve as a crucial building block for groundbreaking discoveries.

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  • Procurenet Team Tshim Sha Tsui
    Hong Kong Hong Kong 3 years

9-Fluorenylmethyl N-hydroxycarbamate

Unlock the versatile potential of 9-Fluorenylmethyl N-hydroxycarbamate, a remarkable chemical compound that has captured the attention of researchers and scientists worldwide. This labile yet powerful molecule, identified by the CAS number 190656-01-0, holds the key to unlocking groundbreaking advancements in various fields, from pharmaceutical development to chemical synthesis.

At the heart of this compound lies a unique molecular structure, a stereoisomer of the well-known fluorenylmethyl carbamate. Synthesized through the reaction of chloroformate and 9-fluorenone, 9-Fluorenylmethyl N-hydroxycarbamate has demonstrated remarkable efficacy as an antibiotic against tuberculosis in mice, showcasing its potential to combat pressing global health challenges.

The synthesis of this compound involves a meticulous process, starting with the activation of a peptidyl chloride, which is then linked to a hydroxamic acid or carboxylate. This intricate process, spanning from solid-phase synthesis to cellular biosynthesis, highlights the compound's versatility and the depth of knowledge required to harness its full potential.

Unparalleled Purity and Specifications

9-Fluorenylmethyl N-hydroxycarbamate boasts an impressive purity of at least 95%, ensuring reliable and consistent results in your research endeavors. With a molecular weight of 255.27 g/mol and a chemical formula of C15H13NO3, this compound is meticulously crafted to meet the highest standards of quality.

The compound's flash point of 164.5°C and its unique MDL number, MFCD01862911, provide valuable technical details that researchers can leverage to unlock new possibilities in their work. Whether you're exploring pharmaceutical applications, advancing chemical synthesis, or delving into material science, 9-Fluorenylmethyl N-hydroxycarbamate is a versatile tool that can propel your research forward.

Unlocking the Potential

The synthesis of 9-Fluorenylmethyl N-hydroxycarbamate is a testament to the ingenuity and dedication of the scientific community. By harnessing the power of this labile compound, researchers can push the boundaries of what's possible, uncovering new avenues for innovation and discovery.

Embrace the potential of 9-Fluorenylmethyl N-hydroxycarbamate in your next project, and unlock a world of possibilities. Dive into the wealth of technical resources and safety guidelines available to ensure the optimal use and handling of this remarkable chemical compound. Together, let's embark on a journey of scientific exploration, where the boundaries of knowledge are continuously expanded, and groundbreaking advancements are made possible.

  • Name: 9-Fluorenylmethyl N-hydroxycarbamate
  • CAS: 190656-01-0
  • Ref #: 3D-QHA65601
  • Description: 9-Fluorenylmethyl N-hydroxycarbamate is a stereoisomer of fluorenylmethyl carbamate. It is synthesized by the reaction of chloroformate and 9-fluorenone. 9-Fluorenylmethyl N-hydroxycarbamate is a labile compound. It has been shown to be an effective antibiotic against tuberculosis in mice. The synthesis of this compound involves the activation of peptidyl chloride, which is then linked to hydroxamic acid or carboxylate. The synthesis starts with the solid phase and ends with cellular biosynthesis.
  • Molecular Weight: 255.27 g/mol
  • Formula: C15H13NO3
  • Purity: Min. 95%
  • MDL: MFCD01862911
  • Flash point: 164.5 °C
  • Formula: C15H13NO3
  • Mdl: MFCD01862911
  • Molecular weight: 255.27 g/mol
  • Purity: Min. 95%
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