CAS 112513-79-8

5H-Pyrrolo[1,2-a]imidazol-7-ol,6,7-dihydro-(9CI)

Description:

5H-Pyrrolo[1,2-a]imidazol-7-ol, 6,7-dihydro- (9CI), with the CAS number 112513-79-8, is a heterocyclic organic compound characterized by its fused pyrrole and imidazole rings. This compound typically exhibits a bicyclic structure, which contributes to its unique chemical properties. It is known for its potential biological activity, making it of interest in medicinal chemistry and drug development. The presence of hydroxyl (-OH) groups in its structure can influence its solubility and reactivity, often enhancing its interaction with biological targets. Additionally, the dihydro form indicates that it has two hydrogen atoms added to the ring system, which can affect its stability and reactivity. The compound may also exhibit various tautomeric forms due to the presence of nitrogen atoms, which can participate in hydrogen bonding. Overall, 5H-Pyrrolo[1,2-a]imidazol-7-ol, 6,7-dihydro- is a compound of interest for further research in pharmacology and organic synthesis.

Formula: C₆H₈N₂O

6,7-Dihydro-5H-pyrrolo[1,2-a]imidazol-7-ol

CAS: 112513-79-8

Formula: C₆H₈N₂O

Purity: 97%

Color and Shape: Solid

Molecular weight: 124.1405

Ref: IN-DA0039S4

5H,6H,7H-Pyrrolo[1,2-a]imidazol-7-ol

CAS: 112513-79-8

5H,6H,7H-Pyrrolo[1,2-a]imidazol-7-ol

Purity: 98%

Molecular weight: 124.14g/mol

Ref: 54-OR94351

5H,6H,7H-Pyrrolo[1,2-a]imidazol-7-ol

CAS: 112513-79-8

Purity: 97%

Molecular weight: 124.1429977

Ref: 10-F601279

5H,6H,7H-Pyrrolo[1,2-a]imidazol-7-ol

CAS: 112513-79-8

The compound 5H,6H,7H-Pyrrolo[1,2-a]imidazol-7-ol is a chiral molecule that has been synthesized and characterized. It has shown to be an effective catalyst for the activation of alkenes and isatin. The reactivity of this compound is due to its dinuclear nature, which allows for two different reactive sites to come in contact with the substrate. The first site is the azomethine nitrogen, which reacts with electrophiles to form nitrenium ions. The second site is the dimeric macrocycle, which reacts with nucleophiles such as water or alcohols to form imidazolidinones. This reactivity makes this compound useful in organic synthesis because it can activate both alkenes and azomethines.

Formula: C₆H₈N₂O

Purity: Min. 95%

Molecular weight: 124.14 g/mol

Ref: 3D-MEA51379