54415-85-9 Usage
Uses
Used in Pharmaceutical Industry:
1H-PYRROLO[2,3-C]PYRIDIN-2(3H)-ONE is used as a key intermediate in the synthesis of various pharmaceuticals due to its potential to contribute to the development of drugs with anti-cancer, anti-inflammatory, and antimicrobial properties. Its structural attributes make it a valuable component in the design and synthesis of novel therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, 1H-PYRROLO[2,3-C]PYRIDIN-2(3H)-ONE serves as a crucial building block for the development of new agrochemicals, potentially enhancing crop protection and management strategies through its incorporation into pesticides or other agricultural chemicals.
Used in Materials Science:
1H-PYRROLO[2,3-C]PYRIDIN-2(3H)-ONE is utilized as a component in the creation of advanced materials, capitalizing on its chemical properties to engineer materials with specific characteristics for various applications in fields such as electronics, plastics, and composites.
Used in Organic Synthesis:
As a versatile chemical, 1H-PYRROLO[2,3-C]PYRIDIN-2(3H)-ONE is used as a reactant in organic synthesis for the preparation of a wide array of chemical compounds, including those with potential applications in research and industry.
Used in Medicinal Chemistry Research:
In the realm of medicinal chemistry, 1H-PYRROLO[2,3-C]PYRIDIN-2(3H)-ONE is employed as a subject of study for its potential as a drug candidate. Researchers investigate its properties and interactions to understand its therapeutic potential and to develop new drugs based on its structure.
Check Digit Verification of cas no
The CAS Registry Mumber 54415-85-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,4,1 and 5 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 54415-85:
(7*5)+(6*4)+(5*4)+(4*1)+(3*5)+(2*8)+(1*5)=119
119 % 10 = 9
So 54415-85-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H6N2O/c10-7-3-5-1-2-8-4-6(5)9-7/h1-2,4H,3H2,(H,9,10)
54415-85-9Relevant articles and documents
Preparation of 6-azaoxindole (6-azaindol-2(3H)-one) and substituted derivatives
Andreassen, Einar J.,Bakke, Jan M.
, p. 49 - 54 (2007/10/03)
A general synthesis of 6-azaoxindoles, substituted in the 3- and 5-position, has been developed starting from 4-methoxyearbomethyl-3- nitropyridine, via hydrogenation of the nitro group and cyclisation of the resulting 3-amino-4-methoxyearbomethyl-pyridin