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3-Phenyl-5-methoxy-1,2,4-oxadiazole is a chemical compound with the molecular formula C9H7N2O2. It is a heterocyclic molecule containing a 1,2,4-oxadiazole ring, which is a five-membered ring with two oxygen atoms and one nitrogen atom. The compound features a phenyl group (C6H5) attached to the 3-position of the oxadiazole ring and a methoxy group (CH3O) at the 5-position. This organic compound is known for its stability and is often used as a building block in the synthesis of various pharmaceuticals, agrochemicals, and materials science applications due to its ability to form stable derivatives and its potential to influence the properties of the final products.

3201-47-6

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3201-47-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3201-47-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,0 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3201-47:
(6*3)+(5*2)+(4*0)+(3*1)+(2*4)+(1*7)=46
46 % 10 = 6
So 3201-47-6 is a valid CAS Registry Number.

3201-47-6Downstream Products

3201-47-6Relevant academic research and scientific papers

Rh(II)-Catalyzed Transannulation of 1,2,4-Oxadiazole Derivatives with 1-Sulfonyl-1,2,3-triazoles: Regioselective Synthesis of 5-Sulfonamidoimidazoles

Strelnikova, Julia O.,Rostovskii, Nikolai V.,Starova, Galina L.,Khlebnikov, Alexander F.,Novikov, Mikhail S.

, p. 11232 - 11244 (2018/09/06)

An effective method for the synthesis of fully substituted 5-sulfonamidoimidazoles by Rh(II)-catalyzed transannulation of 1,2,4-oxadiazole derivatives with N-sulfonyl-1,2,3-triazoles is reported. The reaction works well with both aromatic 1,2,4-oxadiazoles and 1,2,4-oxadiazol-5-ones providing a flexible approach to N-(alkoxy/amino)carbonyl- and N-alkyl-substituted imidazoles. Both the disclosed reactions are completely regioselective and provide the first examples of a carbenoid-mediated transformation of N,N,O-heterocycles.

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