122476-00-0

Basic information

• Product Name: methyl 2-(19-methoxy-17-methyl-3,6,10,13-tetraoxabicyclo<13.3.1>nonadeca-1(19),15,17-trien-8-ylthio)benzoate
• Synonyms: methyl 2-(19-methoxy-17-methyl-3,6,10,13-tetraoxabicyclo<13.3.1>nonadeca-1(19),15,17-trien-8-ylthio)benzoate
• CAS NO: 122476-00-0
• Molecular Weight: 476.591
• Mol File: 122476-00-0.mol

Chemical Properties

• CAS DataBase Reference: methyl 2-(19-methoxy-17-methyl-3,6,10,13-tetraoxabicyclo<13.3.1>nonadeca-1(19),15,17-trien-8-ylthio)benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 2-(19-methoxy-17-methyl-3,6,10,13-tetraoxabicyclo<13.3.1>nonadeca-1(19),15,17-trien-8-ylthio)benzoate(122476-00-0)
• EPA Substance Registry System: methyl 2-(19-methoxy-17-methyl-3,6,10,13-tetraoxabicyclo<13.3.1>nonadeca-1(19),15,17-trien-8-ylthio)benzoate(122476-00-0)

Safety Data

• Hazardous Substances Data: 122476-00-0(Hazardous Substances Data)

Upstream product

• 122475-98-3 Toluene-4-sulfonic acid 19-methoxy-17-methyl-3,6,10,13-tetraoxa-bicyclo[13.3.1]nonadeca-1⁽¹⁸⁾,15⁽¹⁹⁾,16-trien-8-yl ester 
• 122475-95-0 19-methoxy-17-methyl-8-methylene-3,6,10,13-tetraoxabicyclo<13.3.1>nonadeca-1(19),15,17-triene 
• 122475-97-2 19-methoxy-17-methyl-3,6,10,13-tetraoxabicyclo<13.3.1>nonadeca-1(19),15,17-trien-8-ol 
• 60232-82-8 2,6-bis bromomethyl-4-methylanisole 
• 6327-85-1 2,6-bis(hydroxymethyl)-4-methyl-anisole 
• 28544-88-9 2,2'-(2-methylenepropane-1,3-diyldioxy)bisethanol 
• 186581-53-3 diazomethane 

Downstream Products

• 122475-94-9 methyl 2-(19-methoxy-17-methyl-3,6,10,13-tetraoxabicyclo<13.3.1>nonadeca-1(19),15,17-trien-8-ylsulfinyl)benzoate 

Relevant articles and documents

Synthesis and Properties of Coronands Incorporating Lariat Sulfide and Sulfoxide Groups

A series of 8-substituted 19-methoxy-17-methyl-3,6,10,13-tetraoxabicyclononodeca-1(19),15,17-trienes has been prepared and their complexations with alkali metal and ammonium cations studied.When the 8-substituent contained sulfide functionality weak complexes formed, but hosts with lariat sulfoxide substituents formed complexes - with greatest specificity for lithium ions.