54808-41-2

Basic information

• Product Name: bis(3,5-di-tert-butyl-4-methoxyphenyl)methanone
• Synonyms: bis(3,5-di-tert-butyl-4-methoxyphenyl)methanone
• CAS NO: 54808-41-2
• Molecular Weight: 466.704
• Mol File: 54808-41-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: bis(3,5-di-tert-butyl-4-methoxyphenyl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: bis(3,5-di-tert-butyl-4-methoxyphenyl)methanone(54808-41-2)
• EPA Substance Registry System: bis(3,5-di-tert-butyl-4-methoxyphenyl)methanone(54808-41-2)

Safety Data

• Hazardous Substances Data: 54808-41-2(Hazardous Substances Data)

Upstream product

• 32465-70-6 bis(3,5-di-tert-butyl-4-methoxyphenyl)methane 

Downstream Products

• 197570-78-8 1,1-dimethyl-2,2-bis(3,5-di-tert-butyl-4-methoxyphenyl)ethylene 
• 197570-73-3 [Bis-(3,5-di-tert-butyl-4-methoxy-phenyl)-methylene]-hydrazine 
• 1245747-47-0 (2S,3R)-1-(bis(3,5-di-tert-butyl-4-methoxyphenyl)methyl)-N,3-diphenylaziridine-2-carboxamide 
• 1245747-46-9 (2R,3S)-1-(bis(3,5-di-tert-butyl-4-methoxyphenyl)methyl)-N,3-diphenylaziridine-2-carboxamide 
• 32465-70-6 bis(3,5-di-tert-butyl-4-methoxyphenyl)methane 
• 1072879-55-0 3,3',5,5'-tetra-t-butyl-4,4'-dimethoxy benzhydrylamine 
• 197570-74-4 2,2,7,7-Tetrakis-(3,5-di-tert-butyl-4-methoxy-phenyl)-4,4,8,8-tetramethyl-1,6-dithia-dispiro[2.1.2.1]octane 
• 197570-75-5 1,3-bis(bis-(3,5-di-tert-butyl-4-methoxyphenyl)methylene)-2,2,4,4-tetramethylcyclobutane 
• 197570-76-6 1,3-bis(bis-(3,5-di-tert-butyl-4-hydroxyphenyl)methylene)-2,2,4,4-tetramethylcyclobutane 
• 197570-79-9 1,1-dimethyl-2,2-bis(3,5-di-tert-butyl-4-hydroxyphenyl)ethylene 

Relevant articles and documents

Multicomponent cis- and trans-Aziridinatons in the Syntheses of All Four Stereoisomers of Sphinganine

All four stereoisomers of sphinganine can be synthesized by a multicomponent aziridination of an aldehyde, an amine and an α-diazo carbonyl compound mediated by a BOROX catalyst with high asymmetric induction (≥96% ee). The threo isomers are available from ring-opening of cis-aziridines by an oxygen nucleophile with inversion at the C-3 position and the erythro-isomers are likewise available from trans-aziridines.