1358742-31-0

Basic information

• Product Name: (S)-(1-(2-(2-(3,5-dimethylphenylamino) ethylamino)phenyl)pyrrolidin-2-yl)methanol
• Synonyms: (S)-(1-(2-(2-(3,5-dimethylphenylamino) ethylamino)phenyl)pyrrolidin-2-yl)methanol
• CAS NO: 1358742-31-0
• Molecular Weight: 339.481
• Mol File: 1358742-31-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-(1-(2-(2-(3,5-dimethylphenylamino) ethylamino)phenyl)pyrrolidin-2-yl)methanol(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-(1-(2-(2-(3,5-dimethylphenylamino) ethylamino)phenyl)pyrrolidin-2-yl)methanol(1358742-31-0)
• EPA Substance Registry System: (S)-(1-(2-(2-(3,5-dimethylphenylamino) ethylamino)phenyl)pyrrolidin-2-yl)methanol(1358742-31-0)

Safety Data

• Hazardous Substances Data: 1358742-31-0(Hazardous Substances Data)

Upstream product

• 147-85-3 L-proline 
• 108-69-0 3,5-dimethylaminoaniline 
• 1358742-29-6 (S)-N₁-(2-(2-((tert-butyldimethylsilyloxy)methyl)pyrrolidin-1-yl)phenyl)-N₂-(3,5-dimethylphenyl)oxalamide 
• 1358742-28-5 C₂₂H₂₇N₃O₃ 
• 1018295-15-2 2-(3,5-dimethylphenylamino)-2-oxoacetic acid 
• 1358742-11-6 (S)-2-(2-((tert-butyldimethylsilyloxy)methyl)pyrrolidin-1-yl)aniline 
• 1358742-07-0 (S)-2-(2-(methoxymethyl)pyrrolidin-1-yl)aniline 
• 1358742-08-1 (S)-2-((tert-butyldimethylsilyloxy)methyl)-1-(2-nitrophenyl)pyrrolidine 
• 1358742-06-9 (S)-2-(methoxymethyl)-1-(2-nitrophenyl)-pyrrolidine 
• 333441-77-3 2-(3,5-dimethylphenylamino)-2-oxoacetic acidethyl ester 

Downstream Products

• 1358742-32-1 (S)-N₁-(3,5-dimethylphenyl)-N₂-(2-(2-(methoxymethyl)pyrrolidin-1-yl)phenyl)ethane-1,2-diamine 

Relevant articles and documents

Synthesis of amino acid derived imidazolidinium salts as new NHC precatalysts

The preparation of new chiral symmetrically and unsymmetrically N,N′-disubstituted imidazolium based NHC salts Ib, IIb, IIIa-c and IVc-h from the amino acids l-proline and l-phenylalanine, is reported. Some preliminary tests have been carried out, demonstrating that the chiral NHCs give chiral induction in organometallic catalysis and can be used as organocatalysts.