892414-50-5 Usage
Description
1H-Pyrrolo[2,3-b]pyridine, 6-chloro-4-nitro-3-(trifluoromethyl)is a chemical compound with the formula C10H6ClF3N2O2. It belongs to the pyrrolopyridine family and contains a chlorine atom, a nitro group, and a trifluoromethyl group. 1H-Pyrrolo[2,3-b]pyridine, 6-chloro-4-nitro-3-(trifluoroMethyl)is commonly used in the pharmaceutical industry for the synthesis of various drugs and biologically active molecules.
Uses
Used in Pharmaceutical Industry:
1H-Pyrrolo[2,3-b]pyridine, 6-chloro-4-nitro-3-(trifluoroMethyl)is used as a building block in organic synthesis for the development of new drugs and biologically active molecules. Its unique structure and functional groups make it a valuable component in the creation of novel therapeutic agents.
Used in Anti-cancer Applications:
1H-Pyrrolo[2,3-b]pyridine, 6-chloro-4-nitro-3-(trifluoroMethyl)has been studied for its potential anti-cancer properties, making it a candidate for use as an anti-cancer agent. Its specific mechanism of action and target cancer types are still under investigation.
Used in Anti-inflammatory Applications:
1H-Pyrrolo[2,3-b]pyridine, 6-chloro-4-nitro-3-(trifluoroMethyl)has also been studied for its potential anti-inflammatory properties, suggesting that it could be used as an anti-inflammatory agent to treat various inflammatory conditions.
Used in Antimicrobial Applications:
1H-Pyrrolo[2,3-b]pyridine, 6-chloro-4-nitro-3-(trifluoroMethyl)exhibits antimicrobial activity, making it a potential candidate for use in the development of new antimicrobial agents to combat drug-resistant infections.
Check Digit Verification of cas no
The CAS Registry Mumber 892414-50-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,2,4,1 and 4 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 892414-50:
(8*8)+(7*9)+(6*2)+(5*4)+(4*1)+(3*4)+(2*5)+(1*0)=185
185 % 10 = 5
So 892414-50-5 is a valid CAS Registry Number.
892414-50-5Relevant articles and documents
Improved synthesis of the selective rho-kinase inhibitor 6-chloro-n4-{3,5-difluoro-4-[(3-methyl-1h-pyrrolo[2,3-b]pyridin-4-yl)oxy]phenyl} pyrimidin-2,4-diamine
Schirok, Hartmut,Paulsen, Holger,Kroh, Walter,Chen, Gang,Gao, Ping
experimental part, p. 168 - 173 (2010/04/29)
A highly potent and selective Rho-kinase inhibitor containing a 7-azaindole moiety has been developed at Bayer Schering Pharma. Herein we disclose details of a significantly improved synthesis of the compound in 8.2% overall yield. Key aspects include cost and safety considerations and the uncommon use of a trifluoromethyl group with controllable reactivity as a masked methyl group.
