5-Fluoro-1-N-propylbenzene-1,2-diamine

Unlock the versatile potential of 5-Fluoro-1-N-propylbenzene-1,2-diamine, a meticulously crafted chemical compound that holds the key to unlocking new frontiers in scientific research and development. This highly pure and specialized molecule, identified by its CAS number 1072928-93-8, boasts a unique combination of fluorine and propyl substituents, making it a valuable asset for researchers across diverse fields.

At the heart of this compound lies a benzene core, adorned with a fluorine atom at the 5-position and a propyl group attached to the nitrogen of the 1,2-diamine moiety. This strategic arrangement of functional groups endows 5-Fluoro-1-N-propylbenzene-1,2-diamine with a distinct chemical profile, opening up a world of possibilities in the realms of pharmaceutical development, agrochemical innovation, and advanced material synthesis.

Pharmaceutical Prowess

In the dynamic world of pharmaceutical research, 5-Fluoro-1-N-propylbenzene-1,2-diamine shines as a versatile building block. Its fluorinated structure and reactive diamine functionality make it a prime candidate for the synthesis of novel drug candidates, targeting a wide spectrum of therapeutic areas. Researchers can harness the compound's unique properties to develop innovative pharmaceuticals with enhanced pharmacological profiles, improved bioavailability, and increased therapeutic efficacy.

The strategic placement of the fluorine atom and the propyl substituent on the benzene ring can lead to the creation of compounds with tailored pharmacokinetic and pharmacodynamic properties, ultimately contributing to the advancement of modern medicine.

Agrochemical Innovations

Beyond the pharmaceutical realm, 5-Fluoro-1-N-propylbenzene-1,2-diamine also finds its niche in the dynamic field of agrochemical development. Its distinct chemical structure and reactivity make it a valuable building block for the synthesis of advanced crop protection agents, such as pesticides and herbicides. The fluorine and propyl moieties can be strategically incorporated into agrochemical formulations, enhancing their potency, selectivity, and environmental compatibility.

By leveraging the unique properties of 5-Fluoro-1-N-propylbenzene-1,2-diamine, researchers can develop innovative agrochemical solutions that address the pressing challenges faced by modern agriculture, promoting sustainable and efficient crop management practices.

Material Science Advancements

The versatility of 5-Fluoro-1-N-propylbenzene-1,2-diamine extends beyond the realms of pharmaceuticals and agrochemicals, as it also finds application in the exciting field of material science. Researchers can harness the compound's distinct chemical structure to engineer novel materials with enhanced performance characteristics, such as improved thermal stability, mechanical strength, or optical properties.

By incorporating 5-Fluoro-1-N-propylbenzene-1,2-diamine into polymers, coatings, or other advanced materials, scientists can unlock new possibilities in areas like energy storage, optoelectronics, and advanced composites. The strategic placement of the fluorine and propyl groups can lead to the creation of materials with tailored functionalities, opening up a world of opportunities for innovative applications.

Technical Specifications

• CAS Number: 1072928-93-8
• Name: 5-Fluoro-1-N-propylbenzene-1,2-diamine
• Reference Number: 3D-XSB92893
• Molecular Formula: C9H13FN2
• Molecular Weight: 168.21 g/mol
• Purity: Minimum 95%
• MDL