799261-61-3

Basic information

• Product Name: (4S,5S)-4-tert-Butyl-5-methoxy-1-((1S,2R,4R)-2-methoxy-7,7-dimethyl-bicyclo[2.2.1]heptane-1-carbonyl)-3-(toluene-4-sulfonyl)-imidazolidin-2-one
• Synonyms: (4S,5S)-4-tert-Butyl-5-methoxy-1-((1S,2R,4R)-2-methoxy-7,7-dimethyl-bicyclo[2.2.1]heptane-1-carbonyl)-3-(toluene-4-sulfonyl)-imidazolidin-2-one
• CAS NO: 799261-61-3
• Molecular Weight: 506.664
• Mol File: 799261-61-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (4S,5S)-4-tert-Butyl-5-methoxy-1-((1S,2R,4R)-2-methoxy-7,7-dimethyl-bicyclo[2.2.1]heptane-1-carbonyl)-3-(toluene-4-sulfonyl)-imidazolidin-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: (4S,5S)-4-tert-Butyl-5-methoxy-1-((1S,2R,4R)-2-methoxy-7,7-dimethyl-bicyclo[2.2.1]heptane-1-carbonyl)-3-(toluene-4-sulfonyl)-imidazolidin-2-one(799261-61-3)
• EPA Substance Registry System: (4S,5S)-4-tert-Butyl-5-methoxy-1-((1S,2R,4R)-2-methoxy-7,7-dimethyl-bicyclo[2.2.1]heptane-1-carbonyl)-3-(toluene-4-sulfonyl)-imidazolidin-2-one(799261-61-3)

Safety Data

• Hazardous Substances Data: 799261-61-3(Hazardous Substances Data)

Upstream product

• 374590-42-8 (4S,5S)-4,5-dimethoxy-1-[(1S,2R)-2-exomethoxyapocamphanecarbonyl]-2-imidazolidinone 
• 98-59-9 p-toluenesulfonyl chloride 
• 799261-59-9 (4S,5S)-4-tert-Butyl-5-methoxy-1-((1S,2R,4R)-2-methoxy-7,7-dimethyl-bicyclo[2.2.1]heptane-1-carbonyl)-imidazolidin-2-one 

Downstream Products

• 799261-87-3 (1S,2S)-1,2-N,N'-bis(p-toluenesulfonylamino)-1,2-di-tert-butylethane 
• 799261-65-7 (4S,5S)-trans-1-p-tolylsulfonyl-4,5-di-tert-butyl-2-imidazolidinone 
• 799261-86-2 N-(2-amino-1-tert-butyl-3,3-dimethyl-butyl)-4-methyl-benzenesulfonamide 
• 799261-63-5 (4S,5S)-5-tert-Butyl-4-methoxy-1-(toluene-4-sulfonyl)-imidazolidin-2-one 

Relevant articles and documents

Enantioselective synthesis of (1S,2S)-1,2-di-tert-butyl and (1R,2R)-1,2-di-(1-adamantyl)ethylenediamines

The enantioselective synthesis of sterically congested C 2-symmetric 1,2-di-tert-butyl and 1,2-di-(1-adamantyl) ethylenediamines was successfully achieved starting from the simple heterocycle, 2-imidazolone. An enantioselective synthesis of ste