Cyclopentanemethanol , 98% , 3637-61-4
Synonym(s):
(Hydroxymethyl)cyclopentane;Cyclopentyl carbinol
CAS NO.：3637-61-4
Empirical Formula: C6H12O
Molecular Weight: 100.16
MDL number: MFCD00001384
EINECS: 222-861-3
| Pack Size | Price | Stock | Quantity |
| 1g | RMB34.40 | In Stock |
|
| 5G | RMB67.20 | In Stock |
|
| 25G | RMB237.60 | In Stock |
|
| 100G | RMB920.00 | In Stock |
|
| others | Enquire |
PRODUCT 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 | n |
| 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) |
Description and Uses
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].
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.
Safety
| Symbol(GHS) |  GHS07 |
| Signal word | Warning |
| Hazard statements | H315-H319-H335-H227 |
| Precautionary statements | P210-P280-P370+P378-P403+P235-P501-P210e-P261-P280a-P305+P351+P338-P405-P501a |
| Risk Statements | 36/37/38 |
| Safety Statements | 23-24/25 |
| RIDADR | 1987 |
| WGK Germany | 3 |
| HS Code | 29061990 |
