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1,2,3-Trifluoro-4-nitrobenzene CAS:771-69-7

1,2,3-Trifluoro-4-nitrobenzene is a chemical compound with the molecular formula C6H3F3NO2. It belongs to the class of nitrobenzenes and features a benzene ring substituted with three fluorine atoms and a nitro group. This colorless solid possesses unique properties that make it suitable for various industrial and scientific applications.


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Application and Effect:

1,2,3-Trifluoro-4-nitrobenzene serves diverse roles in industrial and scientific applications due to its distinctive chemical characteristics. One significant use of this compound lies in its application as an intermediate in organic synthesis, particularly in the production of pharmaceuticals, agrochemicals, and advanced materials. Its reactivity and unique structure enable the introduction of specific functionalities into molecules, contributing to the creation of valuable compounds beneficial for medical, agricultural, and materials science applications. In organic synthesis, 1,2,3-Trifluoro-4-nitrobenzene plays a crucial role as a versatile building block for introducing trifluoromethyl and nitro groups into complex molecules. This capability is valuable in medicinal chemistry for enhancing drug potency, metabolic stability, and modulating biological activities. Additionally, the reactivity of this compound facilitates the modification of biomolecules, enabling the creation of new derivatives with improved pharmacological and chemical properties useful in drug development and chemical research endeavors. Furthermore, 1,2,3-Trifluoro-4-nitrobenzene is employed in the production of specialty and fine chemicals used across various industries. Its unique reactivity and structural features make it valuable for producing high-performance materials, catalysts, and specialty reagents, contributing to advancements in chemical processes and industrial manufacturing. This compound also finds utility in the field of analytical chemistry and spectroscopy. As a derivative of nitrobenzene, 1,2,3-Trifluoro-4-nitrobenzene can be utilized in derivatization reactions to enhance the detectability of certain compounds in analytical techniques such as mass spectrometry and chromatography. The distinct chemical properties of 1,2,3-Trifluoro-4-nitrobenzene provide advantages in sensitivity and selectivity, aiding in the accurate detection and quantification of target analytes, thereby supporting analytical research and applications. Moreover, 1,2,3-Trifluoro-4-nitrobenzene contributes to the development of advanced materials for electronic and optoelectronic applications. Its unique structure is instrumental in designing organic compounds with tailored electronic properties, enabling the fabrication of functional materials for applications such as organic light-emitting diodes (OLEDs), photovoltaic cells, and organic semiconductors. In summary, 1,2,3-Trifluoro-4-nitrobenzene finds extensive usage across pharmaceutical, chemical, materials, and analytical industries, leveraging its unique structural features and reactivity to enable the creation of valuable compounds and materials for a wide range of practical applications.

Product Sample:

L-Arginine1
L-Arginine2

Product Packing:

L-Arginin3

Additional Information:

Composition C6H3F3NO2
Assay 99%
Appearance white powder
CAS No.  771-69-7
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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