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[(1H-indol-3-yl)-naphth-2-yl-methyl]-methyl-phenyl-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1173282-80-8

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1173282-80-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1173282-80-8 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, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1173282-80:
(9*1)+(8*1)+(7*7)+(6*3)+(5*2)+(4*8)+(3*2)+(2*8)+(1*0)=148
148 % 10 = 8
So 1173282-80-8 is a valid CAS Registry Number.

1173282-80-8Downstream Products

1173282-80-8Relevant 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

A convenient one-pot three component synthesis of 3-aminoalkylated indoles catalyzed by 3-chlorophenylboronic acid

Goswami, Santosh V.,Thorat, Prashant. B.,Kadam, Vijay N.,Khiste, Sachin A.,Bhusare, Sudhakar R.

, p. 422 - 424 (2013/07/04)

An efficient protocol was developed for the synthesis of 3-aminoalkylated indoles using 3-chlorophenylboronic acid as a catalyst under ambient temperature conditions. The three-component reaction of indoles, aromatic aldehydes and N-methyl aniline offered corresponding 3-aminoalkylated indoles in excellent yields. This protocol presents some remarkable features such as mild reaction conditions, simple workup procedure and excellent yields.

PANI-HBF4: A reusable polymer-based solid acid catalyst for three-component, one-pot synthesis of 3-substituted amino methyl indoles under solvent-free conditions

Devi, Chebrolu Lavanya,Rao, Vaidya Jayathirtha,Palaniappan, Srinivasan

experimental part, p. 1593 - 1603 (2012/05/04)

A simple, fast, efficient, high-yielding, and green process is developed for one-pot, three-component synthesis of 3-substituted amino methyl indoles under solvent-free conditions using polyaniline salt as polymer-based reusable solid acid catalyst at room temperature. The advantages of polyaniline salt catalyst are ease of synthesis and handling, low cost, versatality, and recyclability. Copyright Taylor & Francis Group, LLC.

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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