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5-methyl-2-phenyl-indol-3-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

23751-25-9

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23751-25-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23751-25-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,7,5 and 1 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 23751-25:
(7*2)+(6*3)+(5*7)+(4*5)+(3*1)+(2*2)+(1*5)=99
99 % 10 = 9
So 23751-25-9 is a valid CAS Registry Number.

23751-25-9Relevant academic research and scientific papers

Synthesis of N-Fused Seven-Membered Indoline-3-ones via a Palladium-Catalyzed One-Pot Insertion Reaction from 2-Alkynyl Arylazides and Cyclic β-Diketones

Hu, Guiwen,Li, Ping,Sheng, Rong,Zhang, Xiaoxiang,Zhou, Zhiqiang

, (2020)

A novel strategy to synthesize N-fused seven-membered multifunctional polycyclic indoline-3-one derivatives via insertion of cyclic C-acylimines into cyclic β-diketones has been described. The reaction proceeded well under mild reaction conditions via a one-pot, three-steps method, which has shown good tolerance of various functional groups.

Catalytic Asymmetric Mukaiyama-Mannich Reaction of Cyclic C-Acylimines with Difluoroenoxysilanes: Access to Difluoroalkylated Indolin-3-ones

Li, Jin-Shan,Liu, Yong-Jie,Zhang, Guang-Wu,Ma, Jun-An

supporting information, p. 6364 - 6367 (2017/12/08)

A catalytic enantioselective Mukaiyama-Mannich reaction of cyclic C-acylimines with difluoroenoxysilanes is reported. (S)-TRIP enables the enantioselective synthesis of a series of novel difluoroalkylated indolin-3-ones bearing a quaternary stereocenter i

Facile synthesis of 2-aryl-3H-indol-3-ones via singlet oxygenation of 2-arylindoles

Ling

, p. 3831 - 3835 (2007/10/03)

2-Aryl-3H-indole-3-ones have been synthesized via singlet oxygenation of 2-arylindoles in methanol followed by thermodemethoxylation of the resulting 2-aryl-2-methoxy-1,2-dihydro-3H-indol-3-ones in one pot in good yields.

Synthesis and Reactions of 2-Phenylindol-3-ones

Hiremath, Shivayogi P.,Biradar, Jaiprakash S.,Mruthyunjayaswamy, B. H. M.

, p. 308 - 310 (2007/10/02)

2-Phenyl-3-aminoindoles (2a-d) have been synthesised and converted into the corresponding 2-phenylindol-3-ones (4a-d), which on reaction with o-phenylenediamine (5a,b) and nitrostyrene give 9-substituted 5H-5a,6-dihydro-5a-phenylindoloquinoxalines

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