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C-[3-(4-nitro-phenyl)-[1,2,4]oxadiazol-5-yl]-methylamine is a chemical compound characterized by a central oxadiazole ring and a nitrophenyl group. It is a derivative of methylamine and is widely used in research and pharmaceutical applications. The oxadiazole ring is known for its strong fluorescence properties, making C-[3-(4-nitro-phenyl)-[1,2,4]oxadiazol-5-yl]-methylamine valuable for various fluorescence-based assays and imaging techniques. Furthermore, the nitrophenyl group provides specific chemical reactivity and bioactivity to the compound, enhancing its utility in different applications.

90323-86-7

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90323-86-7 Usage

Uses

Used in Research and Pharmaceutical Applications:
C-[3-(4-nitro-phenyl)-[1,2,4]oxadiazol-5-yl]-methylamine is used as a fluorophore in research and pharmaceutical applications due to its strong fluorescence properties. This characteristic makes it an ideal candidate for fluorescence-based assays and imaging techniques, allowing for the detection and monitoring of various biological processes.
Used in Chemical Probes:
In the field of chemical biology, C-[3-(4-nitro-phenyl)-[1,2,4]oxadiazol-5-yl]-methylamine is employed as a chemical probe. The nitrophenyl group confers specific chemical reactivity and bioactivity, making it a useful tool for studying the interactions between molecules and their targets, such as enzymes, receptors, or other proteins.
Used in Fluorescence Imaging Techniques:
C-[3-(4-nitro-phenyl)-[1,2,4]oxadiazol-5-yl]-methylamine is utilized as a fluorescent marker in various imaging techniques. Its strong fluorescence allows for the visualization of cellular structures, molecular interactions, and other biological processes at the microscopic level, providing valuable insights into the underlying mechanisms of various diseases and conditions.
Used in Drug Development:
In the pharmaceutical industry, C-[3-(4-nitro-phenyl)-[1,2,4]oxadiazol-5-yl]-methylamine is used as a starting material or intermediate in the synthesis of new drugs. Its unique chemical properties and reactivity make it a promising candidate for the development of novel therapeutic agents with specific targeting capabilities and improved efficacy.
Used in Material Science:
C-[3-(4-nitro-phenyl)-[1,2,4]oxadiazol-5-yl]-methylamine can also be employed in the field of material science, particularly in the development of new materials with enhanced optical, electronic, or sensing properties. The strong fluorescence and chemical reactivity of the compound make it a valuable component in the design and synthesis of advanced materials for various applications, such as sensors, optoelectronic devices, and more.

Check Digit Verification of cas no

The CAS Registry Mumber 90323-86-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,3,2 and 3 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 90323-86:
(7*9)+(6*0)+(5*3)+(4*2)+(3*3)+(2*8)+(1*6)=117
117 % 10 = 7
So 90323-86-7 is a valid CAS Registry Number.

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