4-(5-((Pyrrolidin-1-yl)methyl)-1,2,4-oxadiazol-3-yl)benzaldehyde - 250mg

REF #: 54-OR322828
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Short description

4-(5-((Pyrrolidin-1-yl)methyl)-1,2,4-oxadiazol-3-yl)benzaldehyde

Unlock the versatile potential of 4-(5-((Pyrrolidin-1-yl)methyl)-1,2,4-oxadiazol-3-yl)benzaldehyde, a premium Building Block compound with a CAS number of 1119452-06-0. This high-purity (>97%) chemical boasts a molecular weight of 257.29g/mol, offering a unique blend of reactivity and selectivity for your advanced research and synthesis needs. Crafted with precision, this pale yellow solid form is a valuable addition to your laboratory, providing a versatile platform for a wide range of applications. Harness the power of this exceptional compound and elevate your experiments to new heights, while exercising caution during handling due to its potential hazardous nature. Unlock the door to innovative discoveries with this premium-quality Building Block.

  • CAS: 1119452-06-0
  • Molecular Weight: 257.29g/mol
  • Hazard Information: TBC
$416
Quantity :
  • Procurenet Team Tshim Sha Tsui
    Hong Kong Hong Kong 3 years
Description

4-(5-((Pyrrolidin-1-yl)methyl)-1,2,4-oxadiazol-3-yl)benzaldehyde

Introducing 4-(5-((Pyrrolidin-1-yl)methyl)-1,2,4-oxadiazol-3-yl)benzaldehyde, 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 compound is poised to unlock new frontiers in pharmaceutical development, agrochemical innovation, and beyond.

At the heart of this compound lies a captivating blend of chemical moieties, including a 1,2,4-oxadiazole core, a pyrrolidine substituent, and a benzaldehyde functional group. This intricate design grants 4-(5-((Pyrrolidin-1-yl)methyl)-1,2,4-oxadiazol-3-yl)benzaldehyde a remarkable versatility, making it a valuable asset in the pursuit of groundbreaking discoveries.

Pharmaceutical Research: Unlocking New Therapeutic Possibilities

In the realm of pharmaceutical research, this compound shines as a crucial building block in the synthesis of innovative drug candidates. Its 1,2,4-oxadiazole scaffold, combined with the pyrrolidine moiety, offers a unique structural platform for the development of targeted therapies. Researchers can leverage the compound's distinct properties to design and synthesize novel pharmaceutical compounds that address a wide range of health conditions, from neurological disorders to metabolic diseases.

The benzaldehyde functionality further enhances the compound's versatility, allowing for strategic modifications and derivatizations that can lead to improved pharmacological profiles and enhanced therapeutic efficacy. By harnessing the power of 4-(5-((Pyrrolidin-1-yl)methyl)-1,2,4-oxadiazol-3-yl)benzaldehyde, scientists can unlock new avenues for groundbreaking pharmaceutical breakthroughs.

Agrochemical Innovation: Cultivating Sustainable Solutions

Beyond the pharmaceutical realm, this compound also finds its place in the dynamic world of agrochemicals. Its unique structural features, including the 1,2,4-oxadiazole core and the pyrrolidine substituent, contribute to the development of advanced crop protection agents. Researchers can utilize 4-(5-((Pyrrolidin-1-yl)methyl)-1,2,4-oxadiazol-3-yl)benzaldehyde as a versatile building block to synthesize potent and selective pesticides, herbicides, or fungicides that safeguard crops while minimizing environmental impact.

The compound's adaptability allows for the formulation of innovative agrochemical products that address the evolving challenges faced by modern agriculture. By harnessing the power of 4-(5-((Pyrrolidin-1-yl)methyl)-1,2,4-oxadiazol-3-yl)benzaldehyde, researchers can contribute to the development of sustainable and efficient agricultural solutions, ensuring bountiful harvests and a healthier ecosystem.

Chemical Synthesis: Unlocking New Frontiers

Beyond its pharmaceutical and agrochemical applications, 4-(5-((Pyrrolidin-1-yl)methyl)-1,2,4-oxadiazol-3-yl)benzaldehyde is a valuable tool in the realm of chemical synthesis. Its unique structural features, including the 1,2,4-oxadiazole ring, the pyrrolidine substituent, and the benzaldehyde functionality, make it a versatile reagent for the creation of novel compounds with tailored properties.

Researchers can leverage the compound's reactivity and selectivity to explore new synthetic pathways, leading to the development of materials with enhanced performance characteristics, such as improved thermal stability, mechanical strength, or optical properties. By harnessing the potential of 4-(5-((Pyrrolidin-1-yl)methyl)-1,2,4-oxadiazol-

Specifications
  • Hazard info: TBC
  • Hs code: 99999999
  • Mdl: MFCD12026822
  • Molecular weight: 257.29g/mol
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