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5-Hydroxy-6-trifluoromethylindole is a chemical compound characterized by the presence of a hydroxyl group (-OH) at the 5th position and a trifluoromethyl group (-CF3) at the 6th position of the indole ring. Indole is a bicyclic organic compound consisting of a benzene ring fused to a pyrrole ring, and this specific derivative exhibits unique chemical properties due to the presence of the electron-withdrawing trifluoromethyl group and the electron-donating hydroxyl group. These functional groups can influence the compound's reactivity, solubility, and potential applications in various fields, such as pharmaceuticals, agrochemicals, or materials science. The compound's structure and properties make it a subject of interest for researchers exploring the effects of substituents on indole-based molecules.

288384-61-2

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288384-61-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 288384-61-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,8,3,8 and 4 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 288384-61:
(8*2)+(7*8)+(6*8)+(5*3)+(4*8)+(3*4)+(2*6)+(1*1)=192
192 % 10 = 2
So 288384-61-2 is a valid CAS Registry Number.

288384-61-2Downstream Products

288384-61-2Relevant academic research and scientific papers

QUINAZOLINE DERIVATIVES AS ANGIOGENESIS INHIBITORS

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Page/Page column 106, (2008/06/13)

The invention relates to the use of compounds of the formula I: wherein ring C is an 8, 9, 10, 12 or 13-membered bicyclic or tricyclic moiety which optionally may contain 1-3 heteroatoms selected independently from O, N and S; Z is -O-, -NH-, -S-, -CH2- or a direct bond; n is 0-5; m is 0-3; R represents hydrogen, hydroxy, halogeno, cyano, nitro, trifluoromethyl, C1-3alkyl, C1-3alkoxy, C1-3alkylsulphanyl, -NRR (wherein R and R, which may be the same or different, each represents hydrogen or C1-3alkyl), or RX- (wherein X and R are as defined herein; R represents hydrogen, oxo, halogeno, hydroxy, C1-4alkoxy, C1-4alkyl, C1-4alkoxymethyl, C1-4alkanoyl, C1-4haloalkyl, cyano, amino, C2-5alkenyl, C2-5alkynyl, C1-3alkanoyloxy, nitro, C1-4alkanoylamino, C1-4alkoxycarbonyl, C1-4alkylsulphanyl, C1-4alkylsulphinyl, C1-4alkylsulphonyl, carbamoyl, N-C1-4alkylcarbamoyl, N,N-di(C1-4alkyl)carbamoyl, aminosulphonyl, N-C1-4alkylaminosulphonyl, N,N-di(C1-4alkyl)aminosulphonyl, N-(C1-4alkylsulphonyl)amino, N-(C1-4alkylsulphonyl)-N-(C1-4alkyl)amino, N,N-di(C1-4alkylsulphonyl)amino, a C3-7alkylene chain joined to two ring C carbon atoms, C1-4alkanoylaminoC1-4alkyl, carboxy or a group RX (wherein X and R are as defined herein); and salts thereof, in the manufacture of a medicament for use in the production of an antiangiogenic and/or vascular permeability reducing effect in warm-blooded animals, processes for the preparation of such compounds, pharmaceutical compositions containing a compound of formula I or a pharmaceutically acceptable salt thereof as active ingredient and compounds of formula I. The compounds of formula I and the pharmaceutically acceptable salts thereof inhibit the effects of VEGF, a property of value in the treatment of a number of disease states including cancer and rheumatoid arthritis.

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