359012-05-8

Basic information

• Product Name: 2,7-bis-[5-(1,1-dimethyl-propyl)-2-hydroxy-phenyl]-benzo[lmn][3,8]phenanthroline-1,3,6,8-tetraone
• Synonyms: 2,7-bis-[5-(1,1-dimethyl-propyl)-2-hydroxy-phenyl]-benzo[lmn][3,8]phenanthroline-1,3,6,8-tetraone
• CAS NO: 359012-05-8
• Molecular Weight: 590.676
• Mol File: 359012-05-8.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 2,7-bis-[5-(1,1-dimethyl-propyl)-2-hydroxy-phenyl]-benzo[lmn][3,8]phenanthroline-1,3,6,8-tetraone(CAS DataBase Reference)
• NIST Chemistry Reference: 2,7-bis-[5-(1,1-dimethyl-propyl)-2-hydroxy-phenyl]-benzo[lmn][3,8]phenanthroline-1,3,6,8-tetraone(359012-05-8)
• EPA Substance Registry System: 2,7-bis-[5-(1,1-dimethyl-propyl)-2-hydroxy-phenyl]-benzo[lmn][3,8]phenanthroline-1,3,6,8-tetraone(359012-05-8)

Safety Data

• Hazardous Substances Data: 359012-05-8(Hazardous Substances Data)

Upstream product

• 1357478-57-9 C₅₀H₄₆N₂O₆ 
• 91339-74-1 2-amino-4-tert-amylphenol 
• 81-30-1 1,4,5,8-naphthalenetetracarboxylic dianhydride 

Downstream Products

• 359642-11-8 2,7-bis-[5-(1,1-dimethyl-propyl)-2-(pyridin-3-ylmethoxy)-phenyl]-benzo[lmn][3,8]phenanthroline-1,3,6,8-tetraone 
• 1357478-57-9 C₅₀H₄₆N₂O₆ 
• 1194043-30-5 C₅₂H₄₆N₂O₈ 
• 1194043-32-7 C₆₄H₅₄N₂O₈ 
• 889671-16-3 [2-{7-[2-tert-butoxycarbonylmethoxy-5-(1,1-dimethyl-propyl)-phenyl]-1,3,6,8-tetraoxo-3,6,7,8-tetrahydro-1H-benzo[lmn][3,8]phenanthrolin-2-yl}-4-(1,1-dimethyl-propyl)-phenoxy]-acetic acid tert-butyl ester 

Relevant articles and documents

Rapid screening of a receptor with molecular memory

Atropisomeric receptor 1 can change conformation and maintain the new conformation when heated and cooled in the presence of a guest molecule. This molecular memory can be used as a rapid method of screening potential guests. Heating atropisomeric diacid

Solvent-induced reversible solid-state colour change of an intramolecular charge-transfer complex

A dynamic intramolecular charge-transfer (CT) complex was designed that displayed reversible colour changes in the solid-state when treated with different organic solvents. The origins of the dichromatism were shown to be due to solvent-inclusion, which induced changes in the relative orientations of the donor pyrene and acceptor naphthalenediimide units.

A high-barrier molecular balance for studying face-to-face arene-arene interactions in the solid state and in solution

An atropisomeric molecular balance was developed to study faceto-face arene-arene interactions. The balance has a large central 1,4,5,8naphthalene diimide surface that forms intramolecular arene-arene interactions with two pendent arms. The balance adopts