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Cyclopentanemethanol

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Cyclopentanemethanol manufacturers

  • Cyclopentanemethanol
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  • CAS:3637-61-4
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  • Purity: 99%
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  • Cyclopentanemethanol
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  • $0.00 / 25KG
  • 2025-03-21
  • CAS:3637-61-4
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Cyclopentanemethanol Basic information
Product Name:Cyclopentanemethanol
Synonyms:RARECHEM AL BD 0721;TIMTEC-BB SBB008516;CYCLOPENTANEMETHANOL;CYCLOPENTYLCARBINOL;(hydroxymethyl)-cyclopentane;Cyclopentylmethyl alcohol;Cyclopentanemethanol, 97+%;Cyclopentanemethanol,98+%
CAS:3637-61-4
MF:C6H12O
MW:100.16
EINECS:222-861-3
Product Categories:1
Mol File:3637-61-4.mol
Cyclopentanemethanol Structure
Cyclopentanemethanol Chemical Properties
Melting point 121-123 °C(Solv: hexane (110-54-3))
Boiling point 162-163 °C(lit.)
density 0.926 g/mL at 25 °C(lit.)
refractive index n20/D 1.458(lit.)
Fp 144 °F
storage temp. Sealed in dry,Room Temperature
pka15.26±0.10(Predicted)
form Liquid
color Clear colorless
BRN 1919000
InChIKeyISQVBYGGNVVVHB-UHFFFAOYSA-N
LogP1.264 (est)
CAS DataBase Reference3637-61-4(CAS DataBase Reference)
NIST Chemistry ReferenceCyclopentanemethanol(3637-61-4)
Safety Information
Risk Statements 36/37/38
Safety Statements 23-24/25
RIDADR 1987
WGK Germany 3
HS Code 29061990
MSDS Information
ProviderLanguage
Cyclopentanemethanol English
SigmaAldrich English
ACROS English
ALFA English
Cyclopentanemethanol Usage And Synthesis
DescriptionCyclopentanemethanol (CPEM) is a metabolite found in or produced by Saccharomyces cerevisiae. Cyclopentanemethanol can be used as a receptor reagent for the preparation of cyclopentyl methyl β-d -glucoside (CPEM-β-G). The compound was found to have an inhibitory effect on sweet amygdalinase activity (Ki=0.15±0.02 mM). The inhibitory activity of CPEM itself on sweet amygdalinase was weak and uncompetitive type. However, the introduction of glucose molecules as glycosyl groups into CPEM converted its inhibitory type into a competitive one[1].
Chemical PropertiesCLEAR COLOURLESS LIQUID
UsesCyclopentanemethanol was used to study catalytic reduction of 6-bromo-1-hexene by nickel (I) salen electrogenerated at a glassy carbon electrode in acetonitrile containing tetramethylammonium tetrafluoroborate by cyclic voltammetry and controlled-potential electrolysis.
Synthesis Reference(s)Tetrahedron Letters, 26, p. 3643, 1985 DOI: 10.1016/S0040-4039(00)89212-6
References[1] 高田 正保  小川 浩一. 環状アルキルβ- D -グルコピラノシドの酵素合成およびその植物起源 β-グルコシダーゼに対する阻害活性[J]. Journal of applied glycoscience, 2004. DOI:10.5458/JAG.51.197.
Tag:Cyclopentanemethanol(3637-61-4) Related Product Information
Cyclopentanecarbaldehyde 1-CYCLOPENTYL-ETHANONE CYCLOPENTYLACETIC ACID Cyclopentyl methyl ether Cyclopentylboronic acid Cyclopentyl isocyanate Cyclopentanecarboxylic acid Cyclopentanemethanol Methyl 2-cyclopentanonecarboxylate 1-(4-CHLOROPHENYL)-1-CYCLOPENTANECARBOXYLIC ACID Betulinic acid Ferrocenecarboxylic acid Taurodeoxycholic acid sodium salt 1,2,3,4-CYCLOPENTANETETRACARBOXYLIC ACID 1,1'-FERROCENEDICARBOXYLIC ACID Cycloleucine Sodium cholate 1-Phenylcyclopentanecarboxylic acid

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