
CAS 152213-63-3
:1H-Indole-3-Acetic Acid, 6-Bromo-A-Oxo-
Description:
1H-Indole-3-Acetic Acid, 6-Bromo-A-Oxo- is a chemical compound that belongs to the class of indole derivatives, which are known for their diverse biological activities. This compound features an indole ring structure, which is a bicyclic structure composed of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring. The presence of the acetic acid moiety suggests that it may exhibit auxin-like properties, potentially influencing plant growth and development. The bromine substituent at the 6-position of the indole ring can impart unique reactivity and biological activity, making it of interest in both synthetic and medicinal chemistry. Additionally, the presence of the keto group (oxo) may enhance its reactivity and interaction with biological targets. Overall, this compound's structural characteristics suggest potential applications in agricultural chemistry and pharmacology, although specific biological activities would require further investigation through empirical studies.
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 5 products.
6-Bromo-1H-indole-3-acetic acid methyl ester
CAS:Formula:C11H10BrNO2Purity:97%Color and Shape:SolidMolecular weight:268.1066Methyl 2-(6-bromo-1H-indol-3-yl)acetate
CAS:Methyl 2-(6-bromo-1H-indol-3-yl)acetatePurity:97%Molecular weight:268.11g/mol6-Bromo-1H-indole-3-acetic acid methyl ester
CAS:6-Bromo-1H-indole-3-acetic acid methyl esterPurity:≥98%Molecular weight:268.11g/mol6-Bromo-1H-indole-3-acetic acid methyl ester
CAS:<p>6-Bromo-1H-indole-3-acetic acid methyl ester (Methyl 6-Bromoindole-3-acetate) is a marine derived natural products found in Pseudosuberites hyalinus.</p>Formula:C11H10BrNO2Purity:99.74%Color and Shape:SolidMolecular weight:268.11



