(R)-(+)-Benzyl-3-acetylaminopyrrolidine is a chiral compound characterized by its pyrrolidine ring, which is a five-membered nitrogen-containing heterocycle. This substance features a benzyl group and an acetylamino substituent, contributing to its unique chemical properties. The presence of the acetylamino group enhances its potential for biological activity, making it of interest in medicinal chemistry. The chirality of the compound indicates that it exists in two enantiomeric forms, with the (R)-(+)-configuration being the specific form referenced. This stereochemistry can significantly influence the compound's interaction with biological targets, such as enzymes or receptors, thereby affecting its pharmacological profile. The compound is typically synthesized through organic reactions involving amines and carbonyl compounds, and it may exhibit solubility in organic solvents. Its applications may extend to research in drug development, particularly in the synthesis of compounds with potential therapeutic effects. As with many chemical substances, safety and handling precautions should be observed due to its potential biological activity.

(R)-(+)-BENZYL-3-ACETYLAMINOPYRROLIDINE&

114636-33-8: (R)-(+)-Benzyl-3-acetylaminopyrrolidine is a chiral compound characterized by its pyrrolidine ring, which is a five-membered nitrogen-containing heterocycle. This substance features a benzyl group and an acetylamino substituent, contributing to its unique chemical properties. The presence of the acetylamino group enhances its potential for biological activity, making it of interest in medicinal chemistry. The chirality of the compound indicates that it exists in two enantiomeric forms, with the (R)-(+)-configuration being the specific form referenced. This stereochemistry can significantly influence the compound's interaction with biological targets, such as enzymes or receptors, thereby affecting its pharmacological profile. The compound is typically synthesized through organic reactions involving amines and carbonyl compounds, and it may exhibit solubility in organic solvents. Its applications may extend to research in drug development, particularly in the synthesis of compounds with potential therapeutic effects. As with many chemical substances, safety and handling precautions should be observed due to its potential biological activity.

CAS 114636-33-8

(R)-(+)-BENZYL-3-ACETYLAMINOPYRROLIDINE&

Acetamide, N-[(3R)-1-(phenylmethyl)-3-pyrrolidinyl]-

Ref: IN-DA000EVU

(R)-N-(1-Benzylpyrrolidin-3-yl)acetamide

Ref: 54-OR92617

(R)-N-(1-Benzylpyrrolidin-3-yl)acetamide

Ref: 10-F780264