CAS 122454-52-8

benzyl (2S,3aS)-1-[(2R)-2-(1-ethoxycarbonylbutylamino)propanoyl]-2,3,3a,4,5,6,7,7a-octahydroindole-2-carboxylate

Description:

Benzyl (2S,3aS)-1-[(2R)-2-(1-ethoxycarbonylbutylamino)propanoyl]-2,3,3a,4,5,6,7,7a-octahydroindole-2-carboxylate is a complex organic compound characterized by its intricate molecular structure, which includes an octahydroindole core. This compound features multiple stereocenters, indicating that it exists in specific stereoisomeric forms, which can significantly influence its biological activity and interactions. The presence of an ethoxycarbonyl group suggests potential applications in medicinal chemistry, particularly in drug design, as it may enhance solubility and bioavailability. The amino acid-like structure implies that it could interact with biological systems, possibly acting as a peptide mimic. Additionally, the benzyl group may contribute to its lipophilicity, affecting its pharmacokinetic properties. Overall, this compound's unique structural features and functional groups make it a subject of interest in various fields, including pharmaceuticals and organic synthesis, where understanding its reactivity and interactions is crucial for potential applications.

Formula: C₂₆H₃₈N₂O₅

InChI: InChI=1/C26H38N2O5/c1-4-11-21(25(30)32-5-2)27-18(3)24(29)28-22-15-10-9-14-20(22)16-23(28)26(31)33-17-19-12-7-6-8-13-19/h6-8,12-13,18,20-23,27H,4-5,9-11,14-17H2,1-3H3/t18-,20+,21?,22?,23+/m1/s1

Perindopril Benzyl Ester

Controlled Product

CAS: 122454-52-8

Applications Perindopril (P287500) derivative.

Formula: C₂₆H₃₈N₂O₅

Color and Shape: Light Yellow

Molecular weight: 458.59

Ref: TR-P287515

(1S)-Perindopril-d4 Benzyl Ester

Controlled Product

CAS: 122454-52-8

Applications (S)- Epimer derivative.

Formula: C₂₆D₄H₃₄N₂O₅

Color and Shape: Neat

Molecular weight: 462.615

Ref: TR-P287518

Perindopril Benzyl Ester

CAS: 122454-52-8

Formula: C₂₆H₃₈N₂O₅

Molecular weight: 458.60

Ref: ST-EA-CP-P18011

Perindopril benzyl ester

CAS: 122454-52-8

Perindopril is a prodrug that is metabolized to its active form, ramipril. It belongs to the group of angiotensin-converting enzyme inhibitors and is used for the treatment of hypertension. The hydroxy group reacts with benzyl chloride in an organic solvent, forming a molecule with a chloride group. This reaction takes place in a reaction vessel that signifies stereoselectively, meaning only one stereoisomer is produced. Perindopril undergoes an acidic amino function, which makes it more difficult for this drug to be absorbed through the gastrointestinal system. In addition, perindopril binds to thionyl chloride or chlorine in anhydrous sodium, which makes it more soluble in water.

Formula: C₂₆H₃₈N₂O₅

Purity: Min. 95%

Molecular weight: 458.59 g/mol

Ref: 3D-FP26846