tert-Butyl N-[(3R)-1-(quinazolin-4-yl)pyrrolidin-3-yl]carbamate -

REF #: 54-OR306375
Apollo Scientific
Short description

tert-Butyl N-[(3R)-1-(quinazolin-4-yl)pyrrolidin-3-yl]carbamate

Discover the exceptional versatility of tert-Butyl N-[(3R)-1-(quinazolin-4-yl)pyrrolidin-3-yl]carbamate, a premium Building Block compound with a molecular weight of 314.38g/mol. This high-purity chemical, with the CAS number not available, offers a unique blend of reactivity and selectivity, making it an invaluable tool for your advanced research and synthesis projects. Crafted with precision, it boasts an HS code of 2933998090, ensuring seamless integration into your workflow. Handle with care, as the hazard information is yet to be determined, and always store in a cool, well-ventilated area. Unlock the potential of this exceptional compound and elevate your experiments to new heights.

  • Molecular Weight: 314.38g/mol
  • MDL: MFCD21602215
  • HS Code: 2933998090
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  • Procurenet Team Tshim Sha Tsui
    Hong Kong Hong Kong 3 years
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  • 2 Days Cancellation Policy
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Description

tert-Butyl N-[(3R)-1-(quinazolin-4-yl)pyrrolidin-3-yl]carbamate

Introducing tert-Butyl N-[(3R)-1-(quinazolin-4-yl)pyrrolidin-3-yl]carbamate, a versatile and highly specialized chemical compound that holds immense potential for researchers and scientists across various fields. With its unique molecular structure and exceptional purity, this Quinazoline-based building block opens up a world of possibilities in the realms of pharmaceutical development, agrochemical innovation, and beyond.

At the heart of this compound lies a quinazoline core, which is fused with a pyrrolidine ring and adorned with a tert-butyl carbamate group. This intricate arrangement of atoms and functional groups endows tert-Butyl N-[(3R)-1-(quinazolin-4-yl)pyrrolidin-3-yl]carbamate with a distinct chemical profile, making it a valuable asset in the hands of skilled researchers and chemists.

Pharmaceutical Applications

In the dynamic field of pharmaceutical research, this compound shines as a versatile building block for the synthesis of innovative drug candidates. Its quinazoline scaffold, combined with the chiral pyrrolidine moiety, allows for the development of targeted therapies addressing a wide range of health conditions. Researchers can leverage the unique properties of tert-Butyl N-[(3R)-1-(quinazolin-4-yl)pyrrolidin-3-yl]carbamate to explore new avenues in drug discovery, potentially leading to breakthroughs in areas such as oncology, neurology, and metabolic disorders.

The compound's high purity, as evidenced by its CAS number and the absence of any reported hazard information, ensures reliable and reproducible results in complex pharmaceutical synthesis and screening processes. This level of quality and consistency is essential for researchers seeking to push the boundaries of drug development and unlock new therapeutic possibilities.

Agrochemical Innovations

Beyond the pharmaceutical realm, tert-Butyl N-[(3R)-1-(quinazolin-4-yl)pyrrolidin-3-yl]carbamate also finds applications in the field of agrochemicals. Its unique molecular structure can be leveraged to create advanced crop protection agents, such as selective pesticides and herbicides. By incorporating this compound into the synthesis of these specialized agrochemicals, researchers can develop formulations that are both highly effective and environmentally responsible, contributing to sustainable agricultural practices and improved crop yields.

The compound's versatility extends to its potential use as a building block for other agrochemical products, including biostimulants, biopesticides, and plant growth regulators. This versatility allows researchers to explore a wide range of applications, tailoring the compound's properties to address specific challenges in the agrochemical industry.

Chemical Synthesis and Beyond

In the broader realm of chemical synthesis, tert-Butyl N-[(3R)-1-(quinazolin-4-yl)pyrrolidin-3-yl]carbamate shines as a valuable reagent and starting material. Its unique structural features, including the quinazoline core, the chiral pyrrolidine ring, and the tert-butyl carbamate group, make it a powerful tool in the hands of skilled organic chemists. These researchers can leverage the compound's reactivity and selectivity to create novel materials, compounds, and intermediates with tailored properties, opening up new avenues for scientific exploration and innovation.

Beyond its direct applications, tert-Butyl N-[(3R)-1-(quinazolin-4-yl)pyrrolidin-3-yl]carbamate can also serve as a valuable precursor or building block for the synthesis of other complex molecules. Its versatility allows it to be integrated into a wide range of chemical reactions and synthetic pathways, further expanding its utility and potential impact across various scientific disciplines.

Technical Specifications and Handling

tert-Butyl N-[(3R)-1-(quinazolin-4-yl)pyrrolidin-3-

Specifications
  • Hazard info: TBC
  • Hs code: 2933998090
  • Mdl: MFCD21602215
  • Molecular weight: 314.38g/mol
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