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6,7-dimethoxy-3-phenyl-2H-benzo[b][1,4]oxazin-2-one is a complex organic compound belonging to the class of benzoxazinones. It features a benzene ring fused to an oxazine ring, with a carbonyl group at position 2. The molecule is characterized by the presence of two methoxy groups at positions 6 and 7, and a phenyl group at position 3. This chemical structure endows the compound with unique properties and potential applications in various fields, such as pharmaceuticals, agrochemicals, and materials science. The specific reactivity, stability, and biological activity of 6,7-dimethoxy-3-phenyl-2H-benzo[b][1,4]oxazin-2-one can be influenced by the electronic and steric effects of the substituents, making it an interesting subject for further research and development.

7134-72-7

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7134-72-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7134-72-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,3 and 4 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7134-72:
(6*7)+(5*1)+(4*3)+(3*4)+(2*7)+(1*2)=87
87 % 10 = 7
So 7134-72-7 is a valid CAS Registry Number.

7134-72-7Relevant academic research and scientific papers

Hypervalent Iodine(III)-Promoted Radical Oxidative C-H Annulation of Arylamines with α-Keto Acids

Long, Lipeng,Wang, Jieyan,Gu, Liuqing,Yang, Shiguang,Qiao, Liang,Luo, Guotian,Chen, Zhengwang

, p. 12084 - 12092 (2021)

A novel catalyst-free radical oxidative C-H annulation reaction of arylamines with α-keto acids toward benzoxazin-2-ones synthesis under mild conditions was developed. This hypervalent iodine(III)-promoted process eliminated the use of a metal catalyst or additive with high levels of functional group tolerance. Hypervalent iodine(III) was both an oxidant and a radical initiator for this reaction. The synthetic utility of this method was confirmed by the synthesis of the natural product cephalandole A.

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