Product Name:8-bromo-3H-oxazolo[4,5-c]quinolin-2-one

IUPAC Name:8-bromo-2H,3H-[1,3]oxazolo[4,5-c]quinolin-2-one

CAS:61428-41-9
Molecular Formula:C10H5BrN2O2
Purity:95%+
Catalog Number:CM390843
Molecular Weight:265.07

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CM390843-1g 1-2 Weeks ǕɅƱ
CM390843-5g 3-4 Weeks ŴƙȁŴ

For R&D use only.

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Product Details

CAS NO:61428-41-9
Molecular Formula:C10H5BrN2O2
Melting Point:-
Smiles Code:BrC1=CC2C3=C(C=NC=2C=C1)NC(=O)O3
Density:
Catalog Number:CM390843
Molecular Weight:265.07
Boiling Point:
MDL No:
Storage:

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Product Overview 8-bromo-3H-oxazolo[4,5-c]quinolin-2-one is a heterocyclic compound that has recently gained attention in scientific research due to its potential applications in various fields. This compound has been synthesized using different methods and has been studied for its mechanism of action, biochemical and physiological effects, advantages, and limitations for lab experiments.
Synthesis and Application 8-bromo-3H-oxazolo[4,5-c]quinolin-2-one has been synthesized using various methods, including the reaction of 8-bromo-2-chloroquinoline with glycine in the presence of triethylamine, and the reaction of 8-bromoquinoline-2-carbaldehyde with glycine in the presence of ammonium acetate. The synthesized compound has been characterized using various spectroscopic techniques such as NMR, IR, and MS. 8-bromo-3H-oxazolo[4,5-c]quinolin-2-one has been studied for its potential applications in various fields such as medicinal chemistry, biochemistry, and pharmacology. This compound has been found to have anticancer, antiviral, and antibacterial activities. It has also been studied for its potential use as a fluorescent probe for detecting DNA damage.
Future Directions There are several future directions for the study of 8-bromo-3H-oxazolo[4,5-c]quinolin-2-one. One of the future directions is to study the structure-activity relationship of this compound to identify more potent analogs. Another future direction is to study the mechanism of action of this compound in more detail to understand its potential applications in various fields. Additionally, this compound can be studied for its potential use as a fluorescent probe for detecting DNA damage. Finally, this compound can be studied for its potential use in combination therapy with other anticancer drugs to enhance their efficacy.