93629-15-3

Basic information

• Product Name: Benzene, 5-(bromomethyl)-1,3-bis(1,1-dimethylethyl)-2-methoxy-
• Synonyms: 3,5-di-tert-butyl-4-methoxybenzyl bromide;4-methoxy-3,5-di-tert-butylbenzyl bromide
• CAS NO: 93629-15-3
• Molecular Formula: C16H25BrO
• Molecular Weight: 313.278
• Mol File: 93629-15-3.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Benzene, 5-(bromomethyl)-1,3-bis(1,1-dimethylethyl)-2-methoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 5-(bromomethyl)-1,3-bis(1,1-dimethylethyl)-2-methoxy-(93629-15-3)
• EPA Substance Registry System: Benzene, 5-(bromomethyl)-1,3-bis(1,1-dimethylethyl)-2-methoxy-(93629-15-3)

Safety Data

• Hazardous Substances Data: 93629-15-3(Hazardous Substances Data)

Upstream product

• 1518-53-2 1,3-di-tert-butyl-2-methoxy-5-methylbenzene 
• 1516-95-6 2,6-di-tert-butyl-anisole 
• 1516-96-7 4-bromo-2,6-di-tert-butylanisole 
• 74684-38-1 2-(3-(tert-butyl)-5-formylphenyl)-2-methylpropanenitrile 
• 93629-17-5 (3,5-di-tert-butyl-4-methoxyphenyl)methanol 
• 128-08-5 N-Bromosuccinimide 
• 128-37-0 2,6-di-tert-butyl-4-methyl-phenol 

Downstream Products

• 1261146-15-9 (1E,3E)-1,4-bis(3,5-di-tert-butyl-4-methoxyphenyl)buta-1,3-diene 

Relevant articles and documents

Phospholane-Phosphite Ligands for Rh Catalyzed Enantioselective Conjugate Addition: Unusually Reactive Catalysts for Challenging Couplings

The use of Rh catalysts derived from a phospholane-phosphite ligand were found to be more productive than the classic rhodium/BINAP system in enantioselective conjugate additions. These catalysts enable the use of lower amounts of aryl boronic acid in an

Amphipathic compound containing hindered phenol and phosphite, synthetic method and application thereof

The invention relates to an amphipathic compound which is composed of a hindered phenol unit, a phosphite unit, a crown ether unit and a straight-chain segment unit. The synergistic effect is controlled by controlling the length of the straight-chain segm

Amphipathic compound containing hindered phenol and pentaerythritol phosphite, synthetic method and application thereof

An amphipathic compound containing both anti-static and anti-oxidizing functional groups is composed of a hindered phenol unit, a pentaerythritol phosphite unit, a crown ether unit and a straight-chain segment unit. The synergistic effect is controlled by controlling the length of the straight-chain segment unit to regulate the distance from the hindered phenol to the pentaerythritol phosphite units, and meanwhile, the content of effective functional groups in unit mass of the compound and the compatibility between the compound and resin are also controlled. Through migration of the crown ether group, the hindered phenol unit and the phosphite unit are migrated to the surface of the resin, so that oxidization in air can be eliminated more effectively. Because the hindered phenol unit and the pentaerythritol phosphite unit have large space structures, so that the crown ether structure is prevented from falling off from the surface of the resin, thereby increasing anti-static time of the compound. The compound can be used as an anti-static and anti-oxidizing agent for polypropylene or polyethylene.