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5-Methoxy-3-methyl-4-phenylisoxazole is a heterocyclic organic compound characterized by the presence of an isoxazole ring, which is a five-membered ring containing three carbon atoms and two oxygen atoms. This specific compound features a methyl group (-CH3) at the 3-position, a methoxy group (-OCH3) at the 5-position, and a phenyl group (C6H5) at the 4-position. The combination of these functional groups gives the molecule unique chemical properties and potential applications in various fields, such as pharmaceuticals and agrochemicals, due to its ability to form stable structures and interact with other molecules.

7713-62-4

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7713-62-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7713-62-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,1 and 3 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7713-62:
(6*7)+(5*7)+(4*1)+(3*3)+(2*6)+(1*2)=104
104 % 10 = 4
So 7713-62-4 is a valid CAS Registry Number.

7713-62-4Downstream Products

7713-62-4Relevant academic research and scientific papers

Synthesis of Substituted Indole-3-carboxylates by Iron(II)-Catalyzed Domino Isomerization of 3-Alkyl/aryl-4-aryl-5-methoxyisoxazoles

Bodunov, Vladimir A.,Galenko, Ekaterina E.,Galenko, Alexey V.,Novikov, Mikhail S.,Khlebnikov, Alexander F.

, p. 2784 - 2798 (2018/06/08)

The iron(II)-catalyzed domino isomerization of 3-alkyl/aryl-4-arylisoxazoles provides a selective access to a wide range of structurally diverse highly substituted indole-3-carboxylates. The operational simplicity, high atom efficiency, and the use of stable starting materials and an inexpensive and low-toxicity catalyst are some of the attractive features of this tandem double ring-opening-ring-closure strategy.

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