- Cyclopentanemethanol
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- $10.00 / 1KG
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2026-01-05
- CAS:3637-61-4
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: 10 mt
- Cyclopentanemethanol
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- $530.00 / 180kg
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2025-08-18
- CAS:3637-61-4
- Min. Order: 1440kg
- Purity: 99%
- Supply Ability: 28.8
- Cyclopentanemethanol
-
- $5.00 / 1kg
-
2025-05-26
- CAS:3637-61-4
- Min. Order: 1kg
- Purity: 0.99
- Supply Ability: 10000
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| | 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.) | | Fp | 144 °F | | storage temp. | Sealed in dry,Room Temperature | | pka | 15.26±0.10(Predicted) | | form | Liquid | | 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) |
| Risk Statements | 36/37/38 | | Safety Statements | 23-24/25 | | RIDADR | 1987 | | WGK Germany | 3 | | HS Code | 29061990 | | Storage Class | 10 - Combustible liquids |
| | 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. |
| | Cyclopentanemethanol Preparation Products And Raw materials |
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