(6-Bromo-1H-indol-2-yl)methanol is a chemical compound characterized by its indole structure, which is a bicyclic compound consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring. The presence of a bromine atom at the 6-position of the indole ring introduces significant electrophilic properties, making it a useful intermediate in organic synthesis. The methanol functional group (-CH2OH) attached to the indole nitrogen enhances its reactivity and solubility in polar solvents. This compound may exhibit biological activity, potentially serving as a scaffold for drug development, particularly in the fields of medicinal chemistry and pharmacology. Its molecular structure allows for various interactions with biological targets, which can be explored in research settings. Additionally, the compound's stability and reactivity can be influenced by the bromine substituent, making it a subject of interest for further studies in synthetic and medicinal chemistry. As with many organic compounds, safety precautions should be observed when handling this substance due to its potential biological effects.

(6-BROMO-1H-INDOL-2-YL)METHANOL

923197-75-5: (6-Bromo-1H-indol-2-yl)methanol is a chemical compound characterized by its indole structure, which is a bicyclic compound consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring. The presence of a bromine atom at the 6-position of the indole ring introduces significant electrophilic properties, making it a useful intermediate in organic synthesis. The methanol functional group (-CH2OH) attached to the indole nitrogen enhances its reactivity and solubility in polar solvents. This compound may exhibit biological activity, potentially serving as a scaffold for drug development, particularly in the fields of medicinal chemistry and pharmacology. Its molecular structure allows for various interactions with biological targets, which can be explored in research settings. Additionally, the compound's stability and reactivity can be influenced by the bromine substituent, making it a subject of interest for further studies in synthetic and medicinal chemistry. As with many organic compounds, safety precautions should be observed when handling this substance due to its potential biological effects.

(6-Bromo-1H-indol-2-yl)methanol

<p>6-Bromo-2-(hydroxymethyl)-1H-indole</p>

CAS 923197-75-5

(6-BROMO-1H-INDOL-2-YL)METHANOL

(6-Bromo-1H-indol-2-yl)methanol

Ref: IN-DA00GUT5

6-Bromo-2-(hydroxymethyl)-1H-indole

Ref: 54-OR16856

(6-Bromo-1H-indol-2-yl)methanol

Ref: 10-F046537