53837-32-4

Basic information

• Product Name: 2-Cyclopentene-1-methanol, 4-hydroxy-, cis-
• CAS NO: 53837-32-4
• Molecular Formula: C6H10O2
• Molecular Weight: 114.144
• Mol File: 53837-32-4.mol

Chemical Properties

• CAS DataBase Reference: 2-Cyclopentene-1-methanol, 4-hydroxy-, cis-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Cyclopentene-1-methanol, 4-hydroxy-, cis-(53837-32-4)
• EPA Substance Registry System: 2-Cyclopentene-1-methanol, 4-hydroxy-, cis-(53837-32-4)

Safety Data

• Hazardous Substances Data: 53837-32-4(Hazardous Substances Data)

Upstream product

• 50-00-0 formaldehyd 
• 542-92-7 cyclopenta-1,3-diene 
• 58101-60-3 methyl cyclopent-3-ene-1-carboxylate 
• 25125-21-7 4-(hydroxymethyl)cyclopentene 

Downstream Products

• 118353-05-2 (+/-)-cis-2-amino-1,9-dihydro-9-[4-(hydroxymethyl)-2-cyclopenten-1-yl]-6H-purin-6-one 
• 118237-75-5 (+/-)-1-(4'β-Hydroxymethylcyclopent-2'-en-1'β-yl)-5-methyl-2,4(1H,3H)-pyrimidinedione 
• 76909-92-7 trans-1-hydroxymethyl-2-hydroxy-3-cyclopentene 
• 76909-91-6 rel-(1R,5R)-5-(hydroxymethyl)cyclopent-2-en-1-ol 
• 54112-42-4 trans-4-Hydroxy-2-cyclopenten-1-methanol 
• 111292-59-2 exo-5-(Benzyloxy)-2-oxabicyclo<2.2.1>heptan 

Relevant articles and documents

Deamination Reactions, 49. - Decomposition of 2-Oxa-5- and -6-norbornanediazonium Ions

The reactivity of 2-oxa-6-norbornanediazonium ions (19, 20) conforms to that of the analogous brosylates (7, 11).Photolysis of the tosylhydrazone 17 in aqueous sodium hydroxide yields 2-oxa-exo-6-norbornanol (15) with no endo isomer 22.The deuterium incor

Cyclit-Reaktionen, II. Darstellung von Bausteinen zur Synthese carbocyclischer Furanose-Analoga

The four isomeric hydroxycyclopentenmethanols 6a to 9a can easily be made by allylhydroxylation of the epoxides 2 and 4 with phenyl selenide.In a second way the pair 8a and 9a has been synthesized from 11 via 15.As the preparation of 20 demonstrates, the functionalisation of 6a to 9a to carbocyclic furanoses is possible.The dicarboxylic diethyl esters 23 and 33 can be converted into models for carbocyclic ketofuranoses.