CAS 32501-05-6
:1,3-Dihydro-2H-pyrrolo[3,2-b]pyridin-2-one
Description:
1,3-Dihydro-2H-pyrrolo[3,2-b]pyridin-2-one, identified by its CAS number 32501-05-6, is a heterocyclic organic compound featuring a fused pyrrole and pyridine structure. This compound typically exhibits a bicyclic framework, which contributes to its unique chemical properties. It is characterized by its nitrogen-containing rings, which can influence its reactivity and potential biological activity. The presence of the carbonyl group in the structure may also impart specific functional properties, such as the ability to participate in hydrogen bonding or act as a site for further chemical modifications. This compound is of interest in medicinal chemistry due to its potential pharmacological applications, including antimicrobial and anticancer activities. Additionally, its structural features may allow for interactions with various biological targets, making it a candidate for drug development. However, detailed studies on its toxicity, stability, and specific applications are necessary to fully understand its utility in various fields.
Formula:C7H6N2O
InChI:InChI=1/C7H6N2O/c10-7-4-6-5(9-7)2-1-3-8-6/h1-3H,4H2,(H,9,10)
InChI key:InChIKey=IHRRHTILSRVFPW-UHFFFAOYSA-N
SMILES:O=C1CC=2C(N1)=CC=CN2
Synonyms:- 1,3-Dihydropyrrolo[3,2-b]pyridin-2-one
- 1H,2H,3H-pyrrolo[3,2-b]pyridin-2-one
- 2H-pyrrolo[3,2-b]pyridin-2-one, 1,3-dihydro-
- NSC 244253
- 1,3-Dihydro-2H-pyrrolo[3,2-b]pyridin-2-one
- 1,3-Dihydro-2H-pyrrolo[3,2-b]pyridin-2-one ISO 9001:2015 REACH
- 1H,3H-Pyrrolo[3,2-b]pyridin-2-one
- 4-Aza-2-oxindole
- 4-Azaoxindole
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Found 4 products.
1H-Pyrrolo[3,2-b]pyridin-2(3H)-one
CAS:Formula:C7H6N2OPurity:97%Color and Shape:SolidMolecular weight:134.1381H-Pyrrolo[3,2-b]pyridin-2(3H)-one
CAS:<p>1H-Pyrrolo[3,2-b]pyridin-2(3H)-one belongs to a class of heterocyclic compounds that are structurally related to the pyridine ring. It has been shown to inhibit the activity of b-raf and may be used as an anticancer agent. 1H-Pyrrolo[3,2-b]pyridin-2(3H)-one is synthesized from formamide and ammonium acetate by a two step process involving nucleophilic substitution and elimination reactions. It is hypothesized that 1H-Pyrrolo[3,2-b]pyridin-2(3H)-one may have an effect on cancer due to its ability to inhibit protein synthesis.</p>Formula:C7H6N2OPurity:Min. 95%Molecular weight:134.14 g/mol




