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1-Methyl-2-phenyl-1H-indol-3-amine is an organic compound with the molecular formula C16H14N2. It is a derivative of indole, a heterocyclic aromatic organic compound that contains a benzene ring fused to a pyrrole. This specific compound features a methyl group at the 1-position, a phenyl group at the 2-position, and an amino group at the 3-position. It is a white to off-white crystalline solid and is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals. The compound is also of interest in the field of materials science due to its potential use in the development of novel organic materials. Its chemical structure and properties make it a valuable intermediate in the preparation of complex organic molecules.

1859-64-9

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1859-64-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1859-64-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,5 and 9 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1859-64:
(6*1)+(5*8)+(4*5)+(3*9)+(2*6)+(1*4)=109
109 % 10 = 9
So 1859-64-9 is a valid CAS Registry Number.

1859-64-9Relevant academic research and scientific papers

Rh(III)-Catalyzed Tandem Acylmethylation/Nitroso Migration/Cyclization of N-Nitrosoanilines with Sulfoxonium Ylides in One Pot: Approach to 3-Nitrosoindoles

Wu, Yingtao,Pi, Chao,Cui, Xiuling,Wu, Yangjie

, p. 361 - 364 (2020/02/04)

A novel synthesis of 3-nitrosoindoles starting from easily available N-nitrosoanilines and sulfoxonium ylides via Rh(III)-catalyzed acylmethylation and trifluoroacetic acid (TFA)-mediated nitroso transfer/cyclization cascade reaction in one pot has been d

An efficient base-mediated intramolecular condensation of 2-(disubstituted amino)-benzonitriles to 3-aminoindoles

Seong, Churl Min,Park, Chul Min,Choi, Jinil,Park, No Sang

scheme or table, p. 1029 - 1031 (2009/05/27)

A concise and versatile method for the preparation of 3-aminoindoles from 2-(disubstituted amino)-benzonitriles is described, and in situ functionalizations were illustrated.

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