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3-[(1H-indol-3-yl)-(methyl-phenyl-amino)-methyl]-phenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1173282-77-3

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1173282-77-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1173282-77-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,3,2,8 and 2 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1173282-77:
(9*1)+(8*1)+(7*7)+(6*3)+(5*2)+(4*8)+(3*2)+(2*7)+(1*7)=153
153 % 10 = 3
So 1173282-77-3 is a valid CAS Registry Number.

1173282-77-3Downstream Products

1173282-77-3Relevant academic research and scientific papers

Iron mediated one pot three component synthesis of 3-substituted indoles via aerobic iminium ion formation

Singh, Vinay K.,Sharma, Laxmi Kant,Singh, Rana Krishna Pal

supporting information, p. 407 - 410 (2016/01/12)

An efficient and economical method was developed for the synthesis of 3 substituted indoles by a highly efficient one-pot three component coupling reaction of substituted or unsubstituted benzyl alcohol, N-methyl aniline or pyrrolidine, and indoles or sub

One-pot synthesis of 3-[(N-alkylanilino)(aryl)methyl]indoles via a transition metal assisted three-component condensation at room temperature

Brahmachari, Goutam,Das, Suvankar

, p. E140-E145 (2014/11/08)

A simple and highly efficient protocol for the one-pot synthesis of a series of 3-[(N-alkylanilino)(aryl)methyl]indoles has been developed based on low-cost and environmentally benign zirconium oxychloride octahydrate and copper chloride dihydrate catalysts via three-component condensation between indoles, aromatic aldehydes, and N-alkylanilines at room temperature under neat condition. Mild reaction conditions, operational simplicity, high atom-economy, good yields in relatively shorter reaction times, use of low-cost and eco-friendly catalysts are some of the salient features of this protocol. A simple and highly efficient protocol for the one-pot synthesis of a series of 3-[(N-alkylanilino)(aryl)methyl]indoles has been developed based on low-cost and environmentally benign zirconium oxychloride octahydrate and copper chloride dihydrate catalysts via three-component condensation between indoles, aromatic aldehydes, and N-alkylanilines at room temperature under neat condition. Mild reaction conditions, operational simplicity, high atom-economy, good yields in relatively shorter reaction times, and use of low-cost and eco-friendly catalysts are the key advantages of the present protocol.

Zwitterionic-type molten salt: A mild and efficient organocatalyst for the synthesis of 3-aminoalkylated indoles via three-component coupling reaction

Kundu, Dhiman,Bagdi, Avik Kr.,Majee, Adinath,Hajra, Alakananda

scheme or table, p. 1165 - 1167 (2011/06/24)

A general and efficient method has been developed for the synthesis of 3-aminoalkylated indoles by a three-component coupling of indoles, aldehydes, and amines in the presence of a catalytic amount of zwitterionic-type molten salt under solvent-free condi

One-pot three-component coupling reaction: solvent-free synthesis of novel 3-substituted indoles catalyzed by PMA-SiO2

Srihari,Singh, Vinay K.,Bhunia, Dinesh C.,Yadav

experimental part, p. 3763 - 3766 (2009/10/11)

Solvent-free PMA-SiO2-catalyzed synthesis of 3-substituted indole derivatives by a one-pot three-component coupling reaction between aldehyde, N-methyl aniline and indole is described.

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