331625-80-0

Basic information

• Product Name: 2,3,5-tris-O-[(4-methoxyphenyl)methyl]-D-Ribitol
• Synonyms: 2,3,5-tris-O-[(4-methoxyphenyl)methyl]-D-Ribitol
• CAS NO: 331625-80-0
• Molecular Weight: 512.6
• Mol File: 331625-80-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2,3,5-tris-O-[(4-methoxyphenyl)methyl]-D-Ribitol(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3,5-tris-O-[(4-methoxyphenyl)methyl]-D-Ribitol(331625-80-0)
• EPA Substance Registry System: 2,3,5-tris-O-[(4-methoxyphenyl)methyl]-D-Ribitol(331625-80-0)

Safety Data

• Hazardous Substances Data: 331625-80-0(Hazardous Substances Data)

Usage

Molecular structure

2,3,5-tris-O-[(4-methoxyphenyl)methyl]-D-Ribitol consists of a ribitol molecule with three methoxyphenylmethyl groups attached at the 2nd, 3rd, and 5th positions.

Derived from

The compound is derived from D-ribitol, a sugar alcohol.

Potential applications

It has potential applications in medicinal chemistry, particularly in the development of pharmaceuticals and drug delivery systems.

Uses in other fields

It may also have uses in materials science and organic synthesis due to its unique structure and properties.

Need for further research

Further research is needed to fully understand the potential uses and effects of this chemical in various industries.

Upstream product

• 331625-54-8 allyl 2,3,5-tri-O-p-methoxybenzyl-D-ribofuranose 
• 532-20-7 D-Ribose 
• 541546-94-5 allyl α,β-D-ribofuranoside 
• 50-69-1 D-ribose 
• 824-94-2 p-methoxybenzyl chloride 

Downstream Products

• 1451992-81-6 (3R,4S,5R)-4,5-bis-p-methoxybenzyloxy-3-p-methoxybenzyloxymethyl-1,2-dithiane 
• 1451992-80-5 (2R,3S,4R)-2,5-dithioacetyl-1,3,4-tris-p-methoxybenzyloxypentane 
• 1050244-48-8 1,4-anhydro-2,3,5-tri-O-(p-methoxybenzyl)-4-seleno-D-ribitol 
• 331625-81-1 (E)-2-Methyl-pentadec-2-enoic acid (1R,2S,3S)-2,3-bis-(4-methoxy-benzyloxy)-1-(4-methoxy-benzyloxymethyl)-4-trityloxy-butyl ester 
• 331625-57-1 (E)-2-Methyl-pentadec-2-enoic acid (1R,2R,3R)-2,3-bis-(4-methoxy-benzyloxy)-1-(4-methoxy-benzyloxymethyl)-3-methoxycarbonyl-propyl ester 
• 331626-38-1 (E)-2-Methyl-pentadec-2-enoic acid (1S,2R,3R)-2,3-bis-(4-methoxy-benzyloxy)-1-(4-methoxy-benzyloxymethyl)-3-methoxycarbonyl-propyl ester 
• 331625-56-0 (E)-2-Methyl-pentadec-2-enoic acid (1R,2S,3S)-4-hydroxy-2,3-bis-(4-methoxy-benzyloxy)-1-(4-methoxy-benzyloxymethyl)-butyl ester 
• 331626-35-8 (E)-2-Methyl-pentadec-2-enoic acid (1S,2S,3S)-4-hydroxy-2,3-bis-(4-methoxy-benzyloxy)-1-(4-methoxy-benzyloxymethyl)-butyl ester 
• 331625-84-4 (2S,3R,4S)-1,3,4-Tris-(4-methoxy-benzyloxy)-5-trityloxy-pentan-2-ol 
• 541546-97-8 1,4-anhydro-2,3,5-tri-O-p-methoxybenzyl-4-thio-D-ribitol 
• 637741-29-8 (2R,3R,4S)-1,3,4-tris(4-methoxybenzyloxy)-5-(tert-butyldimethylsiloxy)-2-pentanol 
• 331625-55-9 (2R,3R,4S)-1,3,4-Tris-(4-methoxy-benzyloxy)-5-trityloxy-pentan-2-ol 

Relevant articles and documents

Synthesis of Stable NAD+ Mimics as Inhibitors for the Legionella pneumophila Phosphoribosyl Ubiquitylating Enzyme SdeC

Stable NAD+ analogues carrying single atom substitutions in either the furanose ring or the nicotinamide part have proven their value as inhibitors for NAD+-consuming enzymes. To investigate the potential of such compounds to inhibit

An improved large scale synthesis of 1,4-anhydro-4-thio-D-ribitol

An improved large scale synthesis of 1,4-anhydro-4-thio-D-ribitol (4) from D-ribose has been accomplished by combining the O-allyl and O-p-methoxybenzyl protecting groups. Compound 4 was obtained in 31% yield in eight steps with three chromatographic sepa