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3H-Imidazo[4,5-f]quinoline(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

149182-17-2

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149182-17-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 149182-17-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,1,8 and 2 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 149182-17:
(8*1)+(7*4)+(6*9)+(5*1)+(4*8)+(3*2)+(2*1)+(1*7)=142
142 % 10 = 2
So 149182-17-2 is a valid CAS Registry Number.

149182-17-2Downstream Products

149182-17-2Relevant articles and documents

Mild and general one-pot reduction and cyclization of aromatic and heteroaromatic 2-nitroamines to bicyclic 2 H -imidazoles

Hanan, Emily J.,Chan, Bryan K.,Estrada, Anthony A.,Shore, Daniel G.,Lyssikatos, Joseph P.

experimental part, p. 2759 - 2764 (2010/12/25)

A one-pot procedure for the conversion of aromatic and heteroaromatic 2-nitroamines into bicyclic 2H-benzimidazoles is described. The procedure employs formic acid, iron powder, and an additive such as NH4Cl to reduce the nitro group and effect the imidazole cyclization with high-yielding conversions generally within one to two hours. The compatibility with a wide range of functionality demonstrates the general utility of this procedure.

Thiazolyl-benzimidazoles

-

Page/Page column 41, (2008/06/13)

The invention is directed to compounds of formula (1) [image] and pharmaceutically acceptable salts thereof, methods for the preparation thereof, and methods of use thereof.

PREPARATION AND SPECTRAL PROPERTIES OF IMIDAZO- AND TRIAZOLOQUINOLINES WITH ANGULAR RING FUSION

Milata, Viktor,Ilavsky, Dusan,Lesko, Jan

, p. 1068 - 1077 (2007/10/02)

The imidazo- and triazoloquinolines (Va, Vb) and imidazo- and triazoloquinolines (Xa, Xb) have been synthetized by the Gould-Jacobs reaction starting from the quinolinecarboxylic acids II and VII prepared by base catalyzed hydrolysis of the esters I and VI, resp.The decarboxylation of the acids II and VII gives the quinolones III and VIII, resp., which are aromatized to the corresponding chloroquinolines IV and IX.The latter compounds give the azoloquinolines V and X on catalytic reduction.The structure of the condensed heterocyclic compounds with angular ring fusion has been proved by 1H and 13C NMR, IR, UV, and mass spectra.

A Facile Synthesis of 2-Substituted Imidazoquinolines

Reddy, A. Pandu Ranga,Veeranagaiah, V.

, p. 673 - 674 (2007/10/02)

Condensation of quinoline-5,6-diamine (II) with aliphatic and aromatic acids under catalytic and thermal conditions results in the corresponding 2-alkyl/aryl-1H-imidazoquinolines (I).

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