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6-Nitro-3-phenyl-2H-benzo[b][1,4]oxazin-2-one is a complex organic chemical compound with the molecular formula C16H10N2O4. It is a derivative of benzoxazine, a heterocyclic compound with a benzene ring fused to an oxazine ring. The molecule features a nitro group at the 6-position, a phenyl group at the 3-position, and a carbonyl group at the 2-position. 6-nitro-3-phenyl-2H-benzo-[b][1,4]oxazin-2-one is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is typically synthesized through multi-step organic reactions and is used as an intermediate in the preparation of more complex molecules. The compound's properties, such as its stability and solubility, can be influenced by the presence of the nitro and phenyl groups, making it a subject of interest in chemical research and development.

7653-47-6

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7653-47-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7653-47-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,5 and 3 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7653-47:
(6*7)+(5*6)+(4*5)+(3*3)+(2*4)+(1*7)=116
116 % 10 = 6
So 7653-47-6 is a valid CAS Registry Number.

7653-47-6Downstream Products

7653-47-6Relevant academic research and scientific papers

Unexpected TFA-catalyzed tandem reaction of benzo[d]oxazoles with 2-oxo-2-arylacetic acids: Synthesis of 3-aryl-2H-benzo[b][1,4]oxazin-2-ones and cephalandole A

Yan, Shaoxi,Ye, Leping,Liu, Miaochang,Chen, Jiuxi,Ding, Jinchang,Gao, Wenxia,Huang, Xiaobo,Wu, Huayue

, p. 16705 - 16709 (2014/05/06)

A convenient and efficient method for the TFA-catalyzed synthesis of 3-aryl-2H-benzo[b][1,4]oxazin-2-ones via a tandem reaction of benzo[d]oxazoles with 2-oxo-2-arylacetic acids was reported for the first time. The efficiency of this transformation was demonstrated by compatibility with a wide range of functional groups. The synthetic utility of this method was confirmed by the synthesis of the natural product cephalandole A. Moreover, a plausible mechanism for the formation of 3-aryl-2H-benzo[b][1,4]oxazin-2-ones involving ring-opening and cyclization steps is proposed. The present synthetic route to 3-aryl-2H-benzo[b][1,4]oxazin-2-ones could be readily scaled up to gram quantity without difficulty.

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