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1-benzyl-5-chloro-2-phenyl-1H-indole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

702702-64-5

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702702-64-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 702702-64-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,0,2,7,0 and 2 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 702702-64:
(8*7)+(7*0)+(6*2)+(5*7)+(4*0)+(3*2)+(2*6)+(1*4)=125
125 % 10 = 5
So 702702-64-5 is a valid CAS Registry Number.

702702-64-5Downstream Products

702702-64-5Relevant academic research and scientific papers

Selective cyclization of alkynols and alkynylamines catalyzed by potassium tert-butoxide

Li, Deng Yuan,Shi, Ke Ji,Mao, Xiao Feng,Le Zhao, Zheng,Wu, Xin Yan,Liu, Pei Nian

, p. 7022 - 7031 (2015/03/14)

Potassium tert-butoxide (t-BuOK) was found to be an effective catalyst for the cyclization of aromatic alkynols and alkynylamines. In the presence of 10 mol % t-BuOK, a range of alkynols were converted to the corresponding exo-cyclic enol ethers as pure Z

On water phosphine-free palladium-catalyzed room temperature C-H arylation of indoles

Islam, Saidul,Larrosa, Igor

, p. 15093 - 15096 (2013/11/06)

Get on top of your chemistry! An "on water", palladium-catalyzed, phosphine-free direct C-H arylation of indoles, with iodoarenes at 25-30°C, is disclosed (see scheme; TBDMS=N-tert-butyldimethylsilyl ether; SEM=N-2-(trimethylsilyl)ethoxymethyl; Bn=benzyl, Piv=pivabyl). The mildness of the reaction conditions permits the tolerance of a variety of N1-protected indoles.

N-ARYLALKYL-3-AMINOALKOXYINDOLES AND THEIR USE AS 5-HT LIGANDS

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Page 46, (2010/02/07)

The present invention describes substituted 3-Aminoalkoxyindoles, as compounds of the general formula (I), its stereoisomers, its radioisotopes, its geometric forms, its N-oxides, its polymorphs, its pharmaceutically acceptable salts, its pharmaceutically acceptable solvates, its useful bioactive metabolites and any suitable combination of the above. The invention also discloses the processes for preparing such compounds of the general formula (I), its stereoisomers, its radioisotopes, its geometric forms, its N-oxides, its polymorphs, its pharmaceutically acceptable salts, its pharmaceutically acceptable solvates, its useful bio-active metabolites and also includes any suitable combination of the above. Further described are various methods of administering these compounds of general formula (I), i.e. pharmaceutically acceptable dosage forms, their composition and their use in either therapy or diagnosis.

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