52883-35-9

Basic information

• Product Name: Rexamino
• Synonyms: Rexamino
• CAS NO: 52883-35-9
• Molecular Formula: C₉H₁₀N₂O
• Molecular Weight: 162.1885
• Product Categories: Amines;Heterocycles;Intermediates & Fine Chemicals;Metabolites & Impurities;Pharmaceuticals
• Mol File: 52883-35-9.mol

Chemical Properties

• Boiling Point: 291.795°C at 760 mmHg
• Flash Point: 130.273°C
• Appearance: /
• Density: 1.264g/cm³
• Vapor Pressure: 0.002mmHg at 25°C
• Refractive Index: 1.624
• CAS DataBase Reference: Rexamino(CAS DataBase Reference)
• NIST Chemistry Reference: Rexamino(52883-35-9)
• EPA Substance Registry System: Rexamino(52883-35-9)

Safety Data

• Hazardous Substances Data: 52883-35-9(Hazardous Substances Data)

Usage

Uses

Aminorex and Rexamino as metabolites of Levamisole

InChI:InChI=1/C9H10N2O/c10-9-11-8(6-12-9)7-4-2-1-3-5-7/h1-5,8H,6H2,(H2,10,11)

Upstream product

• 506-68-3 bromocyane 
• 20989-17-7 Phenylglycinol 
• 100-42-5 styrene 
• 420-04-2 CYANAMID 

Downstream Products

• 53870-08-9 3-phenyl-2,3,5,6-tetrahydro-oxazolo[3,2-a]pyrimidin-7-one 
• 52883-33-7 6-methyl-3-phenyl-2,3,5,6-tetrahydro-oxazolo[3,2-a]pyrimidin-7-one 
• 261920-68-7 9-methyl-3-phenyl-2,3-dihydrooxazolo[3,2-a]pyrimidin-7-one 
• 261920-64-3 3-phenyl-2,3-dihydrooxazolo[3,2-a]pyrimidin-7-one 

Relevant articles and documents

4,5-Disubstituted-1,3-oxazolidin-2-imine derivatives: A new class of orally bioavailable nitric oxide synthase inhibitor

In our search for a novel class of inducible nitric oxide synthase (iNOS) inhibitors, 1,3-oxazolidin-2-imine was found to weakly inhibit iNOS. Further modifications of this compound resulted in a remarkable increase in both the in vivo and in vitro inhibi

An efficient synthesis of a new series of acyclonucleosides starting from β-amino alcohols

A series of new acyclonucleosides analogues 3 has been synthesized very efficiently in three steps starting from β-amino alcohols 1. The key step of this process is a nucleophilic substitution with various nucleophiles on 2,2'-anhydronucleosides 2. The chemo- and stereoselectivities of this reaction are discussed. AM1 calculations sustained the observed chemoselectivity.

One-pot conversion of alkenes into oxazolines and oxazolidin-2-ones promoted by diphenyl diselenide

Oxazolines or oxazolidin-Zones are produced from the reaction of diphenyl diselenide, ammonium persulfate and trifluoromethanesulfonic acid with alkenes in the presence of MeCN/H2O, NH2CN/H2O or NH2CO2Et.