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10-(3-methylphenyl)phenoxazine is a chemical compound with the molecular formula C15H13NO. It is a derivative of phenoxazine, which is a heterocyclic aromatic compound containing a nitrogen atom in a six-membered ring fused to a benzene ring. The 3-methylphenyl group is attached to the phenoxazine core at the 10th position, which is the carbon atom adjacent to the nitrogen atom. 10-(3-methylphenyl)phenoxazine is known for its fluorescent properties and is used in various applications, including as a fluorescent probe in biochemistry and as a dye in the textile industry. Its chemical structure and properties make it a versatile molecule for research and commercial purposes.

58736-72-4

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58736-72-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58736-72-4 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 2 respectively.
Calculate Digit Verification of CAS Registry Number 58736-72:
(7*5)+(6*8)+(5*7)+(4*3)+(3*6)+(2*7)+(1*2)=164
164 % 10 = 4
So 58736-72-4 is a valid CAS Registry Number.

58736-72-4Downstream Products

58736-72-4Relevant 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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