| Identification | More | [Name]
Cyclopentanemethanol | [CAS]
3637-61-4 | [Synonyms]
CYCLOPENTANEMETHANOL
CYCLOPENTYLCARBINOL
CYCLOPENTYLMETHANOL
RARECHEM AL BD 0721
TIMTEC-BB SBB008516
(hydroxymethyl)-cyclopentane
Cyclopentylmethyl alcohol
Cyclopentanemethanol, 97+%
Cyclopentanemethanol,98+%
(Hydroxymethyl)cyclopentane, Cyclopentyl carbinol
Cyclopentane-1-methanol | [EINECS(EC#)]
222-861-3 | [Molecular Formula]
C6H12O | [MDL Number]
MFCD00001384 | [Molecular Weight]
100.16 | [MOL File]
3637-61-4.mol |
| Chemical Properties | Back Directory | [Appearance]
CLEAR COLOURLESS LIQUID | [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 | [form ]
Liquid | [pka]
15.26±0.10(Predicted) | [color ]
Clear colorless | [BRN ]
1919000 | [InChI]
InChI=1S/C6H12O/c7-5-6-3-1-2-4-6/h6-7H,1-5H2 | [InChIKey]
ISQVBYGGNVVVHB-UHFFFAOYSA-N | [SMILES]
C1(CO)CCCC1 | [LogP]
1.264 (est) | [CAS DataBase Reference]
3637-61-4(CAS DataBase Reference) | [NIST Chemistry Reference]
Cyclopentanemethanol(3637-61-4) |
| Safety Data | Back Directory | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S23:Do not breathe gas/fumes/vapor/spray (appropriate wording to be specified by the manufacturer) .
S24/25:Avoid contact with skin and eyes . | [RIDADR ]
1987 | [WGK Germany ]
3
| [HS Code ]
29061990 | [Storage Class]
10 - Combustible liquids |
| Hazard Information | Back Directory | [Description]
Cyclopentanemethanol (CPEM,3637-61-4) 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(3637-61-4) 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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