75894-05-2

Basic information

• Product Name: 1-bis(1-hydroxy-1-methylethyl)-5-(1,1-dimethylethyl)benzene
• Synonyms: 1-bis(1-hydroxy-1-methylethyl)-5-(1,1-dimethylethyl)benzene
• CAS NO: 75894-05-2
• Molecular Weight: 250.381
• Mol File: 75894-05-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1-bis(1-hydroxy-1-methylethyl)-5-(1,1-dimethylethyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-bis(1-hydroxy-1-methylethyl)-5-(1,1-dimethylethyl)benzene(75894-05-2)
• EPA Substance Registry System: 1-bis(1-hydroxy-1-methylethyl)-5-(1,1-dimethylethyl)benzene(75894-05-2)

Safety Data

• Hazardous Substances Data: 75894-05-2(Hazardous Substances Data)

Upstream product

• 917-54-4 methyllithium 
• 78514-79-1 C₃₁H₄₂O₆S 
• 16308-65-9 dimethyl 5-(tert-butyl)isophthalate 
• 75-16-1 methylmagnesium bromide 
• 99-62-7 1,3-diisopropylbenzene 
• 89784-61-2 1-tert-butyl-3,5-diisopropylbenzene 
• 78514-73-5 C₃₀H₃₉O₆S^(1-)*K⁽¹⁺⁾ 
• 78514-65-5 C₃₀H₄₂O₆S 
• 62558-12-7 bis<2-(1-hydroxy-1-methylethyl)-4-(1,1-dimethylethyl)-6-carbethoxyphenyl> sulphide 
• 75894-03-0 7,7'-dicarbethoxy-5,5'-bis(1,1-dimethylethyl)-3,3,3',3'-tetramethyl-1,1'-spiro<3H-2,1-benzoxathiole> 1-oxide 

Relevant articles and documents

METHOD FOR THE SYNTHESIS OF LOW COST INITIATORS FOR TELECHELIC POLYISOBUTYLENES

A method for the synthesis of 1,3-di(chloropropyl)-5-tert-butyl benzene includes the steps of conducting Friedl-Crafts alkylation of 1,3-diisopropyl benzene by tert-butyl chloride in the presence of an alkylation catalyst to obtain 1-tert-butyl-3,5-diisopropylbenzene; peroxidizing the 1-tert-butyl-3,5-diisopropyl benzene by gaseous oxygen in the presence of a peroxidation catalyst in a basic solution to obtain 1,3-di(peroxypropyl)-5-tert-butylbenzene; reducing the 1,3-di(peroxypropyl)-5-tert-butylbenzene with a reducing agent to 1,3-di(hydroxyl propyl)-5-tert-butylbenzene; and chlorinating the 1,3-di(hydroxypropyl)-5-tert-butylbenzene to obtain 1,3-di(chloropropyl)-5-tert-butyl benzene.

Apical Ligand Preference and Fluxional Behavior of Some Sulfuranes

Sulfides 4, 11, and 12 react with m-chloroperbenzoic acid to form apically unsymmetrically substituted sulfuranes 18-20, respectively, instead of the isomeric symmetrically substituted dialkoxysulfuranes.Rapid equilibration (ΔG*12 deg C = 14.7 kcal mol-1) of isomers of sulfurane 18 is observed and studied by (1)H NMR spectroscopy.An associative mechanism for these interconversion processes is proposed.Potassium salts of 18 and 19 are symmetrical dialkoxysulfuranes 21 and 22, respectively.Other reactions involving these sulfuranes are also reported.