4-tert-Butylcatechol

4-tert-Butylcatechol,in the presence of O2 catalyzed by tyrosinase, yields 4-tert-butyl-o-benzoquinone. Electrochemical oxidation of 4-tert-Butylcatechol in the presence of 4-hydroxycoumarin as nucleophile has been studied using cyclic voltammetry and controlled-potential coulometry. It undergoes electrochemical trimerization via anodic oxidation and mechanism of trimerization has been studied using cyclic voltammetry and controlled-potential coulometry.

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Catalog Number CBB1112363
Molecular Formula (CH3)3CC6H3-1,2-(OH)2
CAS# 98-29-3
Purity >99%
Inchi 1S/C10H14O2/c1-10(2,3)7-4-5-8(11)9(12)6-7/h4-6,11-12H,1-3H3
Inchi Key XESZUVZBAMCAEJ-UHFFFAOYSA-N
SMILES CC(C)(C)c1ccc(O)c(O)c1
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Supplier Page https://www.amerigoscientific.com/4-tert-butylcatechol-item-112363.html

4-tert-Butylcatechol

4-tert-Butylcatechol, in the presence of O2 catalyzed by tyrosinase, yields 4-tert-butyl-o-benzoquinone. Electrochemical oxidation of 4-tert-butylcatechol in the presence of 4-hydroxycoumarin as nucleophile has been studied using cyclic voltammetry and controlled-potential coulometry. It undergoes electrochemical trimerization via anodic oxidation and mechanism of trimerization has been studied using cyclic voltammetry and controlled-potential coulometry.

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Catalog Number CBB1112364
Molecular Formula (CH3)3CC6H3-1,2-(OH)2
CAS# 98-29-3
Purity >97%
Inchi 1S/C10H14O2/c1-10(2,3)7-4-5-8(11)9(12)6-7/h4-6,11-12H,1-3H3
Inchi Key XESZUVZBAMCAEJ-UHFFFAOYSA-N
SMILES CC(C)(C)c1ccc(O)c(O)c1
Size Inquiry
Supplier Page https://www.amerigoscientific.com/4-tert-butylcatechol-item-112364.html