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2(1H)-Quinoxalinone, 6-amino-, also known as 6-aminoquinoxaline-2(1H)-one, is a chemical compound with the molecular formula C8H7N3O. It is an amino derivative of quinoxalinone, featuring a six-membered ring with two nitrogen atoms and one oxygen atom. 2(1H)-Quinoxalinone, 6-aminois widely used in organic synthesis and pharmaceutical research as a building block for the synthesis of various bioactive molecules. It has been studied for its potential therapeutic applications, including as an anti-cancer agent and as a treatment for neurological disorders. Furthermore, it exhibits antimicrobial and antifungal properties, making it a versatile and important compound in the field of medicinal chemistry and drug development.

69904-06-9

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69904-06-9 Usage

Uses

Used in Pharmaceutical Research:
2(1H)-Quinoxalinone, 6-aminois used as a building block in pharmaceutical research for the synthesis of various bioactive molecules. Its unique structure and functional groups make it a valuable component in the development of new drugs with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, 2(1H)-Quinoxalinone, 6-aminoserves as a key intermediate for the preparation of a wide range of chemical compounds. Its reactivity and versatility allow for the formation of various derivatives, which can be further utilized in the synthesis of complex organic molecules.
Used in Anticancer Applications:
2(1H)-Quinoxalinone, 6-aminohas been studied for its potential as an anti-cancer agent. Its ability to interact with biological targets and modulate cellular processes makes it a promising candidate for the development of novel cancer therapies. Research is ongoing to explore its efficacy and mechanism of action in combating various types of cancer.
Used in Treatment of Neurological Disorders:
Due to its potential neuroprotective and neuroregenerative properties, 2(1H)-Quinoxalinone, 6-aminois being investigated as a treatment for neurological disorders. Its ability to modulate neuronal signaling pathways and protect against neurodegeneration makes it a candidate for the development of therapeutic agents for conditions such as Alzheimer's disease, Parkinson's disease, and multiple sclerosis.
Used in Antimicrobial and Antifungal Applications:
2(1H)-Quinoxalinone, 6-aminoexhibits antimicrobial and antifungal properties, making it a potential candidate for the development of new antibiotics and antifungal agents. Its ability to inhibit the growth of various pathogens, including bacteria and fungi, highlights its potential in addressing the growing issue of antibiotic resistance and the need for new antimicrobial therapies.

Check Digit Verification of cas no

The CAS Registry Mumber 69904-06-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,9,0 and 4 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 69904-06:
(7*6)+(6*9)+(5*9)+(4*0)+(3*4)+(2*0)+(1*6)=159
159 % 10 = 9
So 69904-06-9 is a valid CAS Registry Number.

69904-06-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-amino-1H-quinoxalin-2-one

1.2 Other means of identification

Product number -
Other names Kinome_3689

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:69904-06-9 SDS

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