149053-69-0

Basic information

• Product Name: 2-amino-N-(2,6-diisopropylphenyl)acetamide
• Synonyms: 2-amino-N-(2,6-diisopropylphenyl)acetamide
• CAS NO: 149053-69-0
• Molecular Weight: 0
• Mol File: 149053-69-0.mol

Chemical Properties

• CAS DataBase Reference: 2-amino-N-(2,6-diisopropylphenyl)acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-amino-N-(2,6-diisopropylphenyl)acetamide(149053-69-0)
• EPA Substance Registry System: 2-amino-N-(2,6-diisopropylphenyl)acetamide(149053-69-0)

Safety Data

• Hazardous Substances Data: 149053-69-0(Hazardous Substances Data)

Usage

Type of compound

Acetamide derivative

Contains

Amino group, aromatic ring

Usage

Pharmaceutical intermediate, building block in organic synthesis

Known for

Potential medicinal properties, studied for applications in medicine and pharmacology

Potential

Can undergo various chemical reactions, can be modified to produce different derivatives with therapeutic uses.

Upstream product

• 135627-76-8 N-[2,6-bis(1-Methylethyl)phenyl]-2-[(phenylmethyl)amino]acetamide 
• 4530-20-5 BOC-glycine 
• 24544-04-5 2,6-diisopropylbenzenamine 

Downstream Products

• 888705-44-0 N¹-(2,6-diisopropylphenyl)ethane-1,2-diamine 

Relevant articles and documents

Immobilization of an anthracene-tagged ruthenium complex on a 2,4,7-trinitrofluoren-9-one-grafted silica: Efficiency and recyclability in olefin metathesis reactions

An anthracene group was linked to the N-heterocyclic carbene moiety of a M71-SIPr-type Ru complex. The tagged complex thus obtained was immobilized by charge-transfer interactions to a 2,4,7-trinitrofluoren-9-one-grafted passivated silica. The immobilized complex proved to be an efficient olefin metathesis catalyst and was reused five times in a multisubstrate olefin metathesis procedure.

Phosphorus containing compounds as antihypercholesterolemic and antiatherosclerotic agents

Novel phosphorus containing compounds are described, as well as methods for the preparation and pharmaceutical composition of same, which are useful in preventing the intestinal absorption of cholesterol and thus are useful in the treatment of hypercholesterolemia and atherosclerosis.