Cyclopentanemethanol
Cyclopentanemethanol Basic information
- Product Name:
- Cyclopentanemethanol
- Synonyms:
-
- RARECHEM AL BD 0721
- TIMTEC-BB SBB008516
- CYCLOPENTYLMETHANOL
- CYCLOPENTANEMETHANOL
- CYCLOPENTYLCARBINOL
- (hydroxymethyl)-cyclopentane
- Cyclopentylmethyl alcohol
- Cyclopentanemethanol, 97+%
- CAS:
- 3637-61-4
- MF:
- C6H12O
- MW:
- 100.16
- EINECS:
- 222-861-3
- Product Categories:
-
- 1
- Mol File:
- 3637-61-4.mol
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.)
- Flash point:
- 144 °F
- storage temp.
- Sealed in dry,Room Temperature
- pka
- 15.26±0.10(Predicted)
- form
- Liquid
- color
- Clear colorless
- BRN
- 1919000
- InChIKey
- ISQVBYGGNVVVHB-UHFFFAOYSA-N
- LogP
- 1.264 (est)
- CAS DataBase Reference
- 3637-61-4(CAS DataBase Reference)
- NIST Chemistry Reference
- Cyclopentanemethanol(3637-61-4)
MSDS
- Language:English Provider:Cyclopentanemethanol
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
- Language:English Provider:ALFA
Cyclopentanemethanol Usage And Synthesis
Description
Cyclopentanemethanol (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 Properties
CLEAR COLOURLESS LIQUID
Uses
Cyclopentanemethanol 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.
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Cyclopentanemethanol(3637-61-4)Related Product Information
- Cyclopentanecarboxylic acid
- Cyclopentanecarbaldehyde
- 1-CYCLOPENTYL-ETHANONE
- CYCLOPENTYLACETIC ACID
- Cyclopentyl methyl ether
- Cyclopentylboronic acid
- Cyclopentyl isocyanate
- Taurodeoxycholic acid sodium salt
- Ferrocenecarboxylic acid
- Betulinic acid
- 1-(4-CHLOROPHENYL)-1-CYCLOPENTANECARBOXYLIC ACID
- Methyl 2-cyclopentanonecarboxylate
- Cyclopentanemethanol
- 1,2,3,4-CYCLOPENTANETETRACARBOXYLIC ACID
- 1,1'-FERROCENEDICARBOXYLIC ACID
- Cycloleucine
- Sodium cholate
- 1-Phenylcyclopentanecarboxylic acid