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2-(p-nitrophenyl)-5-(methylthio)-1,3,4-oxadiazole is a chemical compound with the molecular formula C9H7N3O3S. It is a derivative of 1,3,4-oxadiazole, a five-membered heterocyclic ring containing two nitrogen atoms and one oxygen atom. The compound features a para-nitrophenyl group attached to the 2-position of the oxadiazole ring and a methylthio group at the 5-position. This molecule is known for its potential applications in various fields, such as pharmaceuticals and materials science, due to its unique chemical structure and properties. The presence of the nitro group and the methylthio group imparts specific reactivity and stability characteristics to the molecule, making it a subject of interest for further research and development.

2951-22-6

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2951-22-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2951-22-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,5 and 1 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2951-22:
(6*2)+(5*9)+(4*5)+(3*1)+(2*2)+(1*2)=86
86 % 10 = 6
So 2951-22-6 is a valid CAS Registry Number.

2951-22-6Downstream Products

2951-22-6Relevant academic research and scientific papers

A Novel Synthesis of Peptide Based on the Photochemistry of 5-Azido-1,3,4-oxadiazoles

Confalone, Pat N.,Woodward, Robert B.

, p. 902 - 906 (2007/10/02)

A novel approach to the synthesis of peptides is described.Various N-protected amino acid hydrazides 17 were converted to the salts 18 by condensation with carbon disulfide in methanolic potassium hydroxide.Thermal cyclization of 18 to the heterocycles 19 was followed by reaction with methyl iodide to yield the sulfides 20.After oxidation of 20 to the corresponding sulfones 21, the title compounds 22 were prepared by treating 21 with sodium azide.Deprotection then yielded the free bases 23.Utilization of 22 and 23 in peptide synthesis, relying on a photochemical degradation of the title heterocycle present in these compounds, is described.The scope and limitations of this new methodology are also discussed.

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