51414-56-3

Basic information

• Product Name: 3β-trityloxycholesterol
• Synonyms: 3β-trityloxycholesterol
• CAS NO: 51414-56-3
• Molecular Weight: 628.982
• Mol File: 51414-56-3.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 3β-trityloxycholesterol(CAS DataBase Reference)
• NIST Chemistry Reference: 3β-trityloxycholesterol(51414-56-3)
• EPA Substance Registry System: 3β-trityloxycholesterol(51414-56-3)

Safety Data

• Hazardous Substances Data: 51414-56-3(Hazardous Substances Data)

Upstream product

• 57-88-5 cholesterol 
• 76-83-5 trityl chloride 
• 57-88-5 cholesterol 
• 87839-57-4 1-(Triphenylmethyl)-4(1H)-pyridon 
• 87839-55-2 2-pyridyl trityl ether 
• 76-84-6 triphenylmethyl alcohol 

Downstream Products

• 66252-72-0 (5-Cholesten-3β-yl)-2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosid 
• 71528-63-7 cholesteryl-O-2,3,4,6-tetra-O-benzyl-β-D-mannopyranose 
• 41736-89-4 cholesteryl-O-2,3,4,6-tetra-O-benzyl-α-D-mannopyranose 
• 143520-25-6 cholesteryl 2,3,4,6-tetra-O-benzoyl-D-β-galactopyranoside 
• 41736-89-4 3-O-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)cholesterol 
• 70753-59-2 O-[2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl]cholesterol 

Relevant articles and documents

Gold(I)-catalyzed synthesis of unsymmetrical ethers using alcohols as alkylating reagents

A microwave-irradiated alcohol-protecting strategy based on gold catalysis utilizing benzyl alcohol, tert-butyl alcohol and triphenylmethanol as alkylating reagents has been developed. This protecting strategy has wide functional group tolerance with satisfactory yields for the majority of the selected alcohols. The mechanism of this transformation was probed with oxygen-18 isotope labelled alcohols assisted by GC-MS techniques and chemical kinetic experiments. This strategy provides an efficient, straightforward and alternative approach to the preparation of benzyl, tert-butyl and trityl ethers in organic synthesis.

Trityl ethers: Molecular bevel gears reporting chirality through circular dichroism spectra

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Regioselective N- or O-Tritylation of 2(1H)-Pyridone - (Triphenylmethyl)pyridones as Tritylation Agents

Tritylation of 2(1H)-pyridone (1) with triphenylmethyl chloride (4) in acetonitrile leads exclusively to N-trityl-2(1H)-pyridone (3a) via the lithium salt 1', whereas 2-pyridyl trityl ether (3b) is the only product from the reaction with the sodium salt 1