1333312-26-7

Basic information

• Product Name: 5-(4-bromobut-1-oxy)-11,17,23-tris(1,1-dimethylethyl)-25,26,27,28-tetrahydroxycalix[4]arene
• CAS NO: 1333312-26-7
• Molecular Weight: 743.822
• Mol File: 1333312-26-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 5-(4-bromobut-1-oxy)-11,17,23-tris(1,1-dimethylethyl)-25,26,27,28-tetrahydroxycalix[4]arene(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(4-bromobut-1-oxy)-11,17,23-tris(1,1-dimethylethyl)-25,26,27,28-tetrahydroxycalix[4]arene(1333312-26-7)
• EPA Substance Registry System: 5-(4-bromobut-1-oxy)-11,17,23-tris(1,1-dimethylethyl)-25,26,27,28-tetrahydroxycalix[4]arene(1333312-26-7)

Safety Data

• Hazardous Substances Data: 1333312-26-7(Hazardous Substances Data)

Upstream product

• 33036-62-3 4-Bromo-1-butanol 
• 104-15-4 toluene-4-sulfonic acid 
• 145986-91-0 2,8,13,19-Tetrakis(1,1-dimethylethyl)-11H,22H-4,6:6,10:15,17:17,21-tetramethanodibenzo<1,10>dioxacyclooctadecin-23,25-dione 

Relevant articles and documents

Calix[4]bis(spirodienone) as a versatile synthon for upper rim alkoxylation of calixarenes and synthesis of novel triazole-based biscalixarene by 'CuAAC' chemistry

The spiro rings of calix[4]bis(spirodienone) have been opened up using various bromofunctionalised alcohols employing a novel ipso nucleophilic substitution of tert-butyl groups by alkoxy groups. Additionally, a route has been paved towards the preparation of triazole-linked biscalixarene via the copper(I)-catalysed modern version of classical Huisgen 1,3-dipolar cycloaddition of alkynyl calixarene and azidocalixarene, derived from the above-mentioned bromo-substituted calixarene.