CAS 50358-63-9
:6-Amino-5-bromoquinoxaline
Description:
6-Amino-5-bromoquinoxaline is a heterocyclic organic compound characterized by its quinoxaline structure, which consists of a fused benzene and pyrazine ring. This compound features an amino group (-NH2) at the 6-position and a bromo substituent at the 5-position of the quinoxaline ring, contributing to its reactivity and potential biological activity. It is typically a solid at room temperature and may exhibit moderate solubility in polar solvents. The presence of the amino group allows for hydrogen bonding, which can influence its interactions in biological systems. 6-Amino-5-bromoquinoxaline has garnered interest in medicinal chemistry due to its potential applications in drug development, particularly in the field of cancer research and as a scaffold for synthesizing various bioactive compounds. Its chemical properties, such as reactivity and stability, can be influenced by the presence of the bromine atom, which can participate in electrophilic substitution reactions. Overall, this compound represents a valuable structure for further exploration in pharmaceutical chemistry.
Formula:C8H6BrN3
InChI:InChI=1/C8H6BrN3/c9-7-5(10)1-2-6-8(7)12-4-3-11-6/h1-4H,10H2
InChI key:InChIKey=IRAOSCSPAYZRJE-UHFFFAOYSA-N
SMILES:BrC=1C2=C(C=CC1N)N=CC=N2
Synonyms:- 5-Bromo-6-Amino Quinoxaline
- 5-Bromo-6-aminoquinoxaline
- 5-Bromo-6-quinoxalinamine
- 5-Bromoquinoxalin-6-Amine
- 6-Quinoxalinamine, 5-bromo-
- 6-Amino-5-bromoquinoxaline
- 6-Amino-5-bromoquinoxaline 98%
- 6-Amino-5-bromoquinoxaline ,98%
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 11 products.
Brimonidine Related Compound A (5-Bromoquinoxalin-6-amine)
CAS:Heterocyclic compounds with nitrogen hetero-atom(s) only, aromatic or modified aromatic, nesoiFormula:C8H6BrN3Color and Shape:Yellow Crystalline PowderMolecular weight:222.974515-Bromoquinoxalin-6-amine
CAS:Formula:C8H6BrN3Purity:96%Color and Shape:SolidMolecular weight:224.05736-Amino-5-bromoquinoxaline
CAS:Compound PDK0245, with CAS No. 50358-63-9, is a fragment molecule that serves as an important scaffold for molecular linking, expansion, and modification. Compound PDK0245 provides a structural basis and research tool for the design and screening of novel drug candidates, and is commonly used in drug discovery, drug synthesis, and related research.Formula:C8H6BrN3Molecular weight:224.05Brimonidine EP Impurity B (Brimonidine USP Related Compound A)
CAS:Formula:C8H6BrN3Color and Shape:Brown SolidMolecular weight:224.066-Amino-5-bromoquinoxaline
CAS:Formula:C8H6BrN3Purity:>98.0%(GC)(T)Color and Shape:Light yellow to Amber to Dark green powder to crystalMolecular weight:224.066-Amino-5-bromoquinoxaline
CAS:<p>Impurity Brimonidine EP Impurity B<br>Applications A metabolite of Brimonidine.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Jeon, Y. T., et al.: Bioorg. Med. Chem. Lett., 5, 2255 (1995),<br></p>Formula:C8H6BrN3Color and Shape:YellowMolecular weight:224.066-Amino-5-bromoquinoxaline
CAS:<p>6-Amino-5-bromoquinoxaline is an inhibitor of serine proteases that has been shown to be effective in cell culture and in wild-type mice. It inhibits the enzyme by binding to the catalytic site, blocking the formation of a covalent bond between polypeptide chain and amino acid substrate. 6-Amino-5-bromoquinoxaline has also been shown to have an inhibitory effect on fibrinogen and polyclonal antibodies and can be used as a buffer for other proteases. In addition, this compound also inhibits caproic acid production from fatty acids via an unknown mechanism.br><br>6-Amino-5-bromoquinoxaline is not active against synthetic substrates or monoclonal antibodies.</p>Formula:C8H6BrN3Purity:Min. 95%Color and Shape:PowderMolecular weight:224.05 g/mol5-Bromoquinoxalin-6-amine
CAS:Formula:C8H6BrN3Purity:96%Color and Shape:SolidMolecular weight:224.061











