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4-(7-aza-1H-indol-1-yl)-benzoic acid ethylester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

934290-80-9

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934290-80-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 934290-80-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,4,2,9 and 0 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 934290-80:
(8*9)+(7*3)+(6*4)+(5*2)+(4*9)+(3*0)+(2*8)+(1*0)=179
179 % 10 = 9
So 934290-80-9 is a valid CAS Registry Number.

934290-80-9Relevant academic research and scientific papers

Iron-catalyzed N-arylation of nitrogen nucleophiles

Correa, Arkaitz,Bolm, Carsten

, p. 8862 - 8865 (2007)

(Chemical Equation Presented) Easy does it! A simple procedure for the N-arylation of nitrogen-containing heterocycles and primary amides relies on a catalyst formed in situ from inexpensive and environmentally benign FeCl 3 and a diamine ligand. The cross-coupling reaction with aryl halides provides N-arylated compounds in high yields (see scheme; R = H, Cl, Me, OMe, CO2Et, F, CF3).

NITROGENATED HETEROCYCLIC COMPOUND AND PHARMACEUTICAL COMPOSITION COMPRISING THE SAME

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Page/Page column 17; 22, (2008/12/06)

The present invention relates to novel compounds having a xanthine oxidase inhibitory effect and an uricosuric effect and pharmaceutical compositions comprising the same as an active ingredient. That is, the present invention relates nitrogen-containing heterocyclic compounds represented by the following general formula (I): wherein Y1 represents N or C(R4) ; Y2 represents N or C(R5) ; R4 and R5 independently represent an alkyl group, a hydrogen atom etc. ; one of R1 and R2 represents an optionally substituted aryl group, an alkoxygroup or an optionally substituted heterocyclic group; the other of R1 and R2 represents a haloalkyl group, a cyanogroup, ahalogenatometc.; and R3 represents a 5-tetrazolyl group or a carboxy group, and pharmaceutically acceptable salts thereof, and pharmaceutical compositions comprising the same as an active ingredient.

SELECTIVE AZOLE PDE10A INHIBITOR COMPOUNDS

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Page/Page column 169-170, (2010/11/29)

The invention pertains to heteroaromatic compounds of the formula I, as defined herein, that serve as effective phosphodiesterase (PDE) inhibitors. In particular, the invention relates to said compounds which are selective inhibitors of PDE10. The invention also relates to pharmaceutical compositions comprising said compounds; and the use of said compounds in a method for treating certain central nervous system (CNS) or other disorders.

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