produkt introduktion
| RARECHEM AL BD 0721;TIMTEC-BB SBB008516;CYCLOPENTYLMETHANOL;CYCLOPENTANEMETHANOL;CYCLOPENTYLCARBINOL;(hydroxymethyl)-cyclopentane;Cyclopentylmethyl alcohol;Cyclopentanemethanol, 97+% | |
| 3637-61-4 | |
| C6H12O | |
| 100.16 | |
| 222-861-3 | |
| 1 | |
| 3637-61-4.mol | |
 |
|
| 121-123 degree (Solv: hexane (110-54-3)) | |
| 162-163 degree (lit.) | |
| 0.926 g/mL at 25 degree (lit.) | |
| n20/D 1.458(lit.) | |
| 144 degree F | |
| 15.26±0.10(Predicted) | |
| 1919000 | |
| ISQVBYGGNVVVHB-UHFFFAOYSA-N | |
| 1.264 (est) | |
| 3637-61-4(CAS DataBase Reference) | |
| Cyclopentanemethanol(3637-61-4) |
| 36/37/38 | |
| 23-24/25 | |
| 1987 | |
| 3 | |
| 29061990 |
| 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 -d -glucoside (CPEM- -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. | |
| Tetrahedron Letters, 26, p. 3643, 1985 10.1016/S0040-4039(00)89212-6 | |
| Cyclopentanecarbaldehyde-->Cyclopentene-3-methanol-->Cycloheptanecarboxylic acid methyl ester-->1,5-HEXADIENE-->Phenol-->Cyclopentene-->Carbon dioxide-->Cyclopentanecarboxylic acid-->Guaiacol-->Cyclohexanol-->Cyclohexene oxide-->Anisole--> | |
| 1,4-DICYCLOHEXYLBENZENE-->2-Methylcyclopentanone-->CYCLOPENTYLACETIC ACID--> |
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Ett par: Olivetol
Nästa: 1,2-Dekandiol
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