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N-(4-fluoro-phenyl)-N-nitroso-glycine is an organic compound with the chemical formula C7H6FN2O3. It is a derivative of glycine, an amino acid, with a 4-fluoro-phenyl group attached to the nitrogen atom and a nitroso group (-N=O) on the other nitrogen atom. N-(4-fluoro-phenyl)-N-nitroso-glycine is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structural features. It is important to note that the compound should be handled with care due to its potential reactivity and the presence of a nitroso group, which can be a source of concern in terms of safety and stability.

5319-46-0

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5319-46-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5319-46-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,1 and 9 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5319-46:
(6*5)+(5*3)+(4*1)+(3*9)+(2*4)+(1*6)=90
90 % 10 = 0
So 5319-46-0 is a valid CAS Registry Number.

5319-46-0Relevant academic research and scientific papers

Novel sydnone derivatives carrying azidomethyl-1,2, 4-oxadiazole unit and their 1,3-dipolar cycloadditions

Dürüst, Ya?ar,Y?ld?z, Elif,Karaku?, Hamza,Kariuki, Benson M.

, p. 660 - 670 (2017)

A series of 1,2,4-oxadiazolymethyl sydnones carrying azido group were synthesized and subjected to react with a variety of alkenic and acetylenic dipolarophilic reagents; N-phenyl maleimide, phenyl vinyl sulfone, and phenyl propiolic acid. All the new products are identified by spectral/physical data including high-resolution mass measurements and X-ray diffraction data.

Synthesis and evaluation of phenyl substituted sydnones as potential DPPH-radical scavengers

Mallur, Shanta G.,Tiwari,Raju, B. China,Babu, K. Suresh,Ali, A. Zehra,Sastry,Rao, J. Madhusudana

, p. 1686 - 1689 (2008/09/19)

A series of phenyl substituted sydnones has been synthesized and their radical-scavenging activity has been studied on DPPH free radical. Out of eighteen compounds screened, nine compounds show interesting activity. A mechanism is presented whereby sydnones scavenge DPPH radical through donating H-atom at 4th-position. Its strong radical-scavenging activity mainly arises from 1, 2, 3-oxadiazolium-5-olate ring. Different substituents and their positions on the phenyl ring differently influence DPPH scavenging activity and therefore, may provide clues to design and develop better free-radical scavenging sydnones with multiple activities.

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