121734-80-3

Basic information

• Product Name: (R,R)-N-(1-Phenylethyl) Ibuprofen AMide
• Synonyms: (R,R)-N-(1-Phenylethyl) Ibuprofen AMide
• CAS NO: 121734-80-3
• Molecular Formula: C21H27NO
• Molecular Weight: 339
• Product Categories: Amines;Aromatics;Chiral Reagents;Impurities;Intermediates & Fine Chemicals;Pharmaceuticals
• Mol File: 121734-80-3.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• Storage Temp.: Refrigerator
• Solubility: Chloroform (Slightly), Methanol (Slightly)
• CAS DataBase Reference: (R,R)-N-(1-Phenylethyl) Ibuprofen AMide(CAS DataBase Reference)
• NIST Chemistry Reference: (R,R)-N-(1-Phenylethyl) Ibuprofen AMide(121734-80-3)
• EPA Substance Registry System: (R,R)-N-(1-Phenylethyl) Ibuprofen AMide(121734-80-3)

Safety Data

• Hazardous Substances Data: 121734-80-3(Hazardous Substances Data)

Usage

Uses

Different sources of media describe the Uses of 121734-80-3 differently. You can refer to the following data:
1. The (R,R)-enantiomer of Ibuprofen (I140000) impurity, an anti-inflammatory
2. The (R,R)-enantiomer of Ibuprofen (I140000) impurity, an anti-inflammatory compound.

Upstream product

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• 859827-67-1 (2R)-2-(4-isobutylphenyl)-N-[(trifluoromethyl)sulfonyl]propanamide 
• 618-36-0 rac-methylbenzylamine 

Relevant articles and documents

BORONIC ACID CATALYSTS AND METHODS OF USE THEREOF FOR ACTIVATION AND TRANSFORMATION OF CARBOXYLIC ACIDS

The present application provides methods and catalysts for activation of carboxylic acids for organic reactions. In particular, methods are disclosed for direct nucleophilic addition reactions, such as, amidation reactions with amines, cycloadditions, and conjugate additions, using boronic acid catalysts of formula I, II or III: Also included are novel boronic acid catalysts of formula IV, V and III:

N-Acyltrifluoromethanesulfonamides as new chemoselective acylating agents for aliphatic and aromatic amines

This work describes advances in the study of the internal condensation of ammonium salts of N-acylsulfonamides. N-Acyltrifluoromethanesulfonamides show considerable advantages over the non fluorinated analogues by virtue of their higher reactivity and aci