437613-72-4

Basic information

• Product Name: N-(tert-butyloxycarbonyl)-N-(formylmethyl)-2,4,6-trimethylphenylamine
• Synonyms: N-(tert-butyloxycarbonyl)-N-(formylmethyl)-2,4,6-trimethylphenylamine
• CAS NO: 437613-72-4
• Molecular Weight: 277.364
• Mol File: 437613-72-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N-(tert-butyloxycarbonyl)-N-(formylmethyl)-2,4,6-trimethylphenylamine(CAS DataBase Reference)
• NIST Chemistry Reference: N-(tert-butyloxycarbonyl)-N-(formylmethyl)-2,4,6-trimethylphenylamine(437613-72-4)
• EPA Substance Registry System: N-(tert-butyloxycarbonyl)-N-(formylmethyl)-2,4,6-trimethylphenylamine(437613-72-4)

Safety Data

• Hazardous Substances Data: 437613-72-4(Hazardous Substances Data)

Upstream product

• 88-05-1 2,4,6-trimethylaniline 
• 56700-69-7 (2,4,6-trimethyl-phenyl)-carbamic acid tert-butyl ester 
• 24424-99-5 di-tert-butyl dicarbonate 
• 437613-71-3 N-(tert-butyloxycarbonyl)-N-(3-methyl-but-2-enyl)-2,4,6-trimethylphenylamine 

Downstream Products

• 627536-34-9 [2-(2'-hydroxy-6'-trifluoromethyl-[1,1']binaphthalenyl-2-ylamino)-ethyl]-(2,4,6-trimethyl-phenyl)-carbamic acid tert-butyl ester 

Relevant articles and documents

Recyclable chiral metathesis catalysts

The present invention relates to chiral metal catalysts for stereoselective olefin metathesis reactions, which are recyclable and reusable in such metathesis reactions. The chiral metal-based metathesis catalysts of the invention comprise multidentate optically active or racemic chiral ligands that enable their use in asymmetric synthetic processes, such as for example, in ring-opening and ring-closing metathesis reactions (ROM and RCM, respectively) of alkenes. The catalysts of the invention are organometallic complexes of multivalent metals comprising one or more chiral bidentate ligands that exhibit superior reactivity and stereoselectivity properties. The present invention also provides methods of making such catalysts and methods for utilizing them in catalyzing stereoselective olefin metathesis reactions to provide asymmetric products in relatively high enantiomeric or stereoisomeric excess.