CAS 676245-12-8

(4-pirrolidin-1-ilfenil)metanol

Fórmula: C₁₁H₁₅NO

InChI: InChI=1/C11H15NO/c13-9-10-3-5-11(6-4-10)12-7-1-2-8-12/h3-6,13H,1-2,7-9H2

SMILES: C1CCN(C1)c1ccc(cc1)CO

Sinónimos:

• [4-(1-Pyrrolidinyl)Phenyl]Methanol
• [4-(Pyrrolidin-1-yl)phenyl]methanol
• Benzenemethanol, 4-(1-Pyrrolidinyl)-
• [4-(pyrrolidin-1-yl)phenyl]methanol - [AC78149]
• (4-PYRROLIDIN-1-YLPHENYL)METHANOL
• 4-(1-Pyrrolidinyl)-benzeneMethanol
• 4-(1-Pyrrolidinyl)benzyl Alcohol
• RARECHEM AL BD 1489

(4-Pyrrolidin-1-ylphenyl)methanol

CAS: 676245-12-8

(4-Pyrrolidin-1-ylphenyl)methanol

Fórmula: C₁₁H₁₅NO

Pureza: 95%

Peso molecular: 177.2429

Ref: 54-OR962644

(4-Pyrrolidin-1-ylphenyl)methanol

CAS: 676245-12-8

Fórmula: C₁₁H₁₅NO

Pureza: 97%

Peso molecular: 177.2429

Ref: IN-DA00G1N4

(4-Pyrrolidin-1-ylphenyl)methanol

CAS: 676245-12-8

Pureza: 97%

Peso molecular: 177.246994

Ref: 10-F635883

(4-Pyrrolidin-1-ylphenyl)methanol

CAS: 676245-12-8

4-Pyrrolidin-1-ylphenol is a protease enzyme inhibitor that has been shown to inhibit the catalytic activity of serine proteases. It reversibly binds to the active site of these enzymes and inhibits their ability to hydrolyze peptide bonds, which are required for protein digestion. 4-Pyrrolidin-1-ylphenol has been shown to be a specific inhibitor of hepatitis C virus protease. This drug has also been used as a reagent in the synthesis of peptides and proteins, and is being investigated as a potential drug in the treatment of HIV infection. 4-Pyrrolidin-1-ylphenol is an asymmetric chiral molecule that can be synthesized using Grignard reaction with benzyl alcohol and an amino phenyl boronic acid. The stereochemistry of this molecule is determined by its molecular modeling and conformational analysis. The amino group in this molecule is orientated such that it

Fórmula: C₁₁H₁₅NO

Pureza: Min. 95%

Peso molecular: 177.25 g/mol

Ref: 3D-BCB24512