149790-52-3

Basic information

• Product Name: Acetic acid 2-(2-acetoxy-5-tert-butyl-benzoyl)-4-tert-butyl-phenyl ester
• Synonyms: Acetic acid 2-(2-acetoxy-5-tert-butyl-benzoyl)-4-tert-butyl-phenyl ester
• CAS NO: 149790-52-3
• Molecular Weight: 410.51
• Mol File: 149790-52-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Acetic acid 2-(2-acetoxy-5-tert-butyl-benzoyl)-4-tert-butyl-phenyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Acetic acid 2-(2-acetoxy-5-tert-butyl-benzoyl)-4-tert-butyl-phenyl ester(149790-52-3)
• EPA Substance Registry System: Acetic acid 2-(2-acetoxy-5-tert-butyl-benzoyl)-4-tert-butyl-phenyl ester(149790-52-3)

Safety Data

• Hazardous Substances Data: 149790-52-3(Hazardous Substances Data)

Upstream product

• 799-13-3 bis(5-tert-butyl-2-hydroxyphenyl)methane 
• 149790-47-6 Acetic acid 2-(2-acetoxy-5-tert-butyl-benzyl)-4-tert-butyl-phenyl ester 

Downstream Products

• 149790-91-0 4-t-butyl-2-<5-t-butyl-3-<5-t-butyl-3-(5-t-butylsalicyl)salicyloyl>salicyl>phenol 
• 149790-66-9 2-bromo-4-t-butyl-6-<5-t-butyl-3-<5-t-butyl-3-(5-t-butylsalicyloyl)salicyl>salicyloyl>phenol 
• 149826-78-8 4-t-butyl-2-(5-t-butyl-3-chloromethylsalicyloyl)-6-chloromethylphenol 
• 25446-98-4 2,2'-dihydroxy-5,5'-di-tert-butylbenzophenone 

Relevant articles and documents

Synthesis and Inclusion Properties of Carbonyl-Bridged Analogs of Acyclic p-t-Butylphenol-Formaldehyde Oligomers

A series of compounds in which a part or all of the methylene bridges of acyclic p-t-butylphenol-formaldehyde oligomers are replaced by C=O bridge(s) has been synthesized.The carbonyl-bridged tetramers, except for that with no methylene bridge, formed crystalline host-guest complexes with various organic compounds; those with two C=O bridges were superior regarding complexation, regardless of the position of the bridges.Exclusive guest selectivity of the tetramer with one terminal C=O bridge was observed for benzene and its methyl derivatives in a two-component system.The fully carbonyl-bridged dimer, trimer, tetramer, and pentamer had no complexing-capability.The thermal stability of benzene complexes (host : guest = 2 : 1) of the tetramers with one C=O bridge, as estimated from their thermal dissociation rates, are remarkably lower than that of the parent tetramer.Oximes derived from the tetramers with one C=O bridge were much more effective than the corresponding carbonyl-bridged ones regarding their complex-forming capability.