180524-82-7

Basic information

• Product Name: (+)-(1S,4S,5S)-4,5-dihydroxy-4,5-O-isopropylidene-1-(p-methoxybenzyloxy)methylcyclopent-2-en-1-ol
• Synonyms: (+)-(1S,4S,5S)-4,5-dihydroxy-4,5-O-isopropylidene-1-(p-methoxybenzyloxy)methylcyclopent-2-en-1-ol
• CAS NO: 180524-82-7
• Molecular Weight: 306.359
• Mol File: 180524-82-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (+)-(1S,4S,5S)-4,5-dihydroxy-4,5-O-isopropylidene-1-(p-methoxybenzyloxy)methylcyclopent-2-en-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (+)-(1S,4S,5S)-4,5-dihydroxy-4,5-O-isopropylidene-1-(p-methoxybenzyloxy)methylcyclopent-2-en-1-ol(180524-82-7)
• EPA Substance Registry System: (+)-(1S,4S,5S)-4,5-dihydroxy-4,5-O-isopropylidene-1-(p-methoxybenzyloxy)methylcyclopent-2-en-1-ol(180524-82-7)

Safety Data

• Hazardous Substances Data: 180524-82-7(Hazardous Substances Data)

Upstream product

• 105-13-5 4-Methoxybenzyl alcohol 
• 88023-83-0 1-methoxy-4-{[(methylsulfanyl)methoxy]methyl}-benzene 
• 104010-72-2 (3aS,6aS)-2,2-dimethyl-3a,6a-dihydro-4H-cyclopenta[d][1,3]dioxol-4-one 
• 88023-78-3 para-methoxybenzyl chloride 

Downstream Products

• 180524-84-9 Acetic acid (3aS,4S,6aR)-6-(4-methoxy-benzyloxymethyl)-2,2-dimethyl-4,6a-dihydro-3aH-cyclopenta[1,3]dioxol-4-yl ester 
• 180524-83-8 Acetic acid (3aS,4S,6aS)-4-(4-methoxy-benzyloxymethyl)-2,2-dimethyl-4,6a-dihydro-3aH-cyclopenta[1,3]dioxol-4-yl ester 

Relevant articles and documents

Carbocyclic analogues of D-ribose-5-phosphate: Synthesis and behavior with 5-phosphoribosyl α-1-pyrophosphate synthetases

The synthesis of cyclopentyl and cyclopentenyl analogues of the α- anomer of D-ribose-5-phosphate from D-ribonolactone and D-ribose is described. These analogues, which have the same absolute configuration as D- ribose-5-phosphate, were incubated with PRPP synthetases in an attempt to prepare the corresponding carbocyclic PRPP analogues. The carbocyclic ribose- 5-phosphate analogues were found to be inhibitors, rather than substrates, for 5-phosphoribosyl α-1-pyrophosphate synthetases of both bacterial and human origin. The inhibitory behavior of the analogues is described.