95870-54-5

Basic information

• Product Name: 1-O-allyl-3-O-triphenylmethylglycerol
• Synonyms: 1-O-allyl-3-O-triphenylmethylglycerol
• CAS NO: 95870-54-5
• Molecular Weight: 374.48
• Mol File: 95870-54-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1-O-allyl-3-O-triphenylmethylglycerol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-O-allyl-3-O-triphenylmethylglycerol(95870-54-5)
• EPA Substance Registry System: 1-O-allyl-3-O-triphenylmethylglycerol(95870-54-5)

Safety Data

• Hazardous Substances Data: 95870-54-5(Hazardous Substances Data)

Upstream product

• 123-34-2 3-allyloxy-1,2-propanediol 
• 76-83-5 trityl chloride 

Downstream Products

• 271789-27-6 2,10-Bis(allyloxymethyl)-1,11-bis(tosyloxy)-3,6,9-trioxaundecane 
• 271789-17-4 2-Allyloxymethyl-1,11-bis(tosyloxy)-3,6,9-trioxaundecane 
• 186766-41-6 2-Allyloxymethyl-1,8-bis(tosyloxy)-3,6-dioxaoctane 
• 170166-16-2 C₅₄H₅₈O₇ 
• 163668-94-8 1-O-allyl-2-O-benzyl-3-O-triphenylmethylglycerol 
• 187839-72-1 2-Allyloxymethyl-4,11,18-tris-(toluene-4-sulfonyl)-1-oxa-4,11,18-triaza-cyclohenicosane 
• 187839-70-9 2-allyloxymethyl-3-oxa-1,6-hexanediol ditosylate 
• 163668-92-6 methyl 3,4,6-tri-O-benzyl-2-O-(2-benzyloxy-6,7-dihydroxy-4-oxaheptyl)-α-D-glucopyranoside 
• 163668-91-5 methyl 3,4,6-tri-O-benzyl-2-O-(2-benzyloxy-6,7-epoxy-4-oxaheptyl)-α-D-glucopyranoside 
• 163668-86-8 methyl 2-O-(3-allyloxy-2-benzyloxypropyl)-3,4,6-tri-O-benzyl-α-D-glucopyranoside 
• 163668-85-7 1-O-allyl-2-O-benzyl-3-O-trifluoromethanesulfonylglycerol 
• 85820-98-0 1-O-allyl-2-O-benzylglycerol 

Relevant articles and documents

Two new methods to form substituted oligoethylene glycols

1-Bromo-2-trityloxyethane (1) and 1-allyloxymethyl-2-trityloxyethanol (2) react readily at room temperature with substituted oligoethylene glycols or the ditosylate derivative of an oligoethylene glycol, respectively, to form the extended, ditrityl-protected, substituted oligoethylene glycols in high yields. The trityl groups are easily removed by acidified methanol in CH2Cl2 to give the extended, substituted oligoethylene glycols.

2,2'-Bipyridine lariat calixcrowns: A new class of encapsulating ligands forming highly luminescent Eu3+ and Tb 3+ complexes

A new class of calix[4]arene crown ethers with one or two bipyridines appended to the polyether ring (lariat calixcrowns) have been designed and synthesized; the luminescence properties of their Eu3+ and Tb3+ complexes have been studied in acetonitrile. In this solvent, long lifetimes for the metal emitting states and high metal-luminescence intensities obtained upon ligand excitation have been observed in both Eu3+ and Tb3+ complexes. The association constants in methanol have been determined for some of the complexes studied.