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

1173282-78-4

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1173282-78-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1173282-78-4 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 8 respectively.
Calculate Digit Verification of CAS Registry Number 1173282-78:
(9*1)+(8*1)+(7*7)+(6*3)+(5*2)+(4*8)+(3*2)+(2*7)+(1*8)=154
154 % 10 = 4
So 1173282-78-4 is a valid CAS Registry Number.

1173282-78-4Downstream Products

1173282-78-4Relevant 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

Micelle promoted multicomponent synthesis of 3-amino alkylated indoles via a Mannich-type reaction in water

Kumar, Atul,Gupta, Maneesh Kumar,Kumar, Mukesh,Saxena, Deepti

, p. 1673 - 1678 (2013/03/13)

An efficient micelle promoted one-pot synthesis of 3-amino alkylated indoles has been developed via a three-component Mannich-type reaction from secondary amines, aldehydes and indoles in water under mild reaction conditions. In this Mannich-type reaction

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

Bromodimethylsulfonium bromide (BDMS)-catalyzed multicomponent synthesis of 3-aminoalkylated indoles

Yadav, Deepak K.,Patel, Rajesh,Srivastava, Vishnu P.,Watal, Geeta,Yadav, Lal Dhar S.

experimental part, p. 5701 - 5703 (2010/11/05)

Bromodimethylsulfonium bromide (BDMS)-catalyzed three-component coupling reaction between indoles, aldehydes, and N-alkylanilines is reported to access substituted 3-aminoalkylated indoles at room temperature in high yields (82-96%) within 1.5-3.5 h. The

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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