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10-(4-methylphenyl)phenoxazine is a chemical compound with the molecular formula C15H13NO. It is a derivative of phenoxazine, which is a heterocyclic aromatic compound consisting of a phenyl ring fused to an oxazine ring. The compound is characterized by the presence of a 4-methylphenyl group attached to the 10th position of the phenoxazine core. This organic molecule is known for its potential applications in various fields, such as in the synthesis of dyes, pharmaceuticals, and other organic compounds. Its chemical structure and properties make it a versatile building block for the development of new materials and compounds with specific functionalities.

58736-73-5

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58736-73-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58736-73-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,7,3 and 6 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 58736-73:
(7*5)+(6*8)+(5*7)+(4*3)+(3*6)+(2*7)+(1*3)=165
165 % 10 = 5
So 58736-73-5 is a valid CAS Registry Number.

58736-73-5Downstream Products

58736-73-5Relevant academic research and scientific papers

Pd-Catalyzed double N-arylation of primary amines to synthesize phenoxazines and phenothiazines

Zhang, Lu,Huang, Xin,Zhen, Shan,Zhao, Jing,Li, Heng,Yuan, Bingxin,Yang, Guanyu

, p. 6306 - 6309 (2017/08/10)

An efficient and versatile Pd-catalyzed tandem C-N bond formation between aryl halides and primary amines is developed. The transformation allows a one-pot synthesis of phenoxazine and phenothiazine derivatives with a broad range of substitution patterns from readily available precursors.

A general route for synthesis of N-aryl phenoxazines via copper(i)-catalyzed N-, N-, and O-arylations of 2-aminophenols

Liu, Nan,Wang, Bo,Chen, Wenwen,Liu, Chulong,Wang, Xinyan,Hu, Yuefei

, p. 51133 - 51139 (2014/12/10)

A novel copper(i)-catalyzed tandem reaction of N- and O-arylations of 2-[N-(2-chlorophenyl)amino]phenols was developed, by which a series of structurally novel N-aryl phenoxazines were synthesized efficiently. This success owes much to the discovery of hi

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