88454-84-6

Basic information

• Product Name: (2R,3R)-N,N,N',N'-Tetramethyl-2,3-bis<2-<2-(benzyloxy)ethoxy>ethyl>tataramide
• CAS NO: 88454-84-6
• Molecular Weight: 560.688
• Mol File: 88454-84-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2R,3R)-N,N,N',N'-Tetramethyl-2,3-bis<2-<2-(benzyloxy)ethoxy>ethyl>tataramide(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,3R)-N,N,N',N'-Tetramethyl-2,3-bis<2-<2-(benzyloxy)ethoxy>ethyl>tataramide(88454-84-6)
• EPA Substance Registry System: (2R,3R)-N,N,N',N'-Tetramethyl-2,3-bis<2-<2-(benzyloxy)ethoxy>ethyl>tataramide(88454-84-6)

Safety Data

• Hazardous Substances Data: 88454-84-6(Hazardous Substances Data)

Upstream product

• 100-39-0 benzyl bromide 
• 64352-98-3 benzyl (2-(2-chloroethoxy)ethyl) ether 
• 2050-25-1 diethylene glycol monobenzyl ether 
• 26549-65-5 N,N,N',N'-tetramethyl L-tartramide 
• 88454-83-5 ((2-(2-iodoethoxy)ethoxy)methyl)benzene 

Relevant articles and documents

Synthesis of Lipophilic 18-Crown-6 Diacids for the Membrane Transport of Alkaline-Earth Cations

The synthesis of three different types of lipophilic 18-crown-6 diacids is described.A didecyl crown ether 2,3-diacid (1) was prepared as a minor product from a diiodide precursor (12) and threo-11,12-docosanediol by thallous ethoxide cyclization.The major nonpolymeric products resulted from elimination followed by cyclization to give 15-crown-5-derivatives.A crown ether 11,12-diamide 2,3-diacid (4) was prepared by a similar route involving cyclization of a benzyl protected precursor (26) and N,N,N',N'-tetramethyltartaramide (9).Isomeric syn and anti 2,11(12)-diamide 3,12(11)-diacid derivatives 6 and 7 were prepared from the known crown ether bisanhydride 8 and alkylamines.The product mixture was separated by chromatography, and the isomers were identified by comparison of acidity and stability constants for complexation with those of closely related syn/anti crown ether acids.