pentyl การใช้

• Replacement of the piperidinyl by pentyl or a heptyl chain gave the compounds agonistic properties.
• The ester formed from 1-pentanol and butyric acid is pentyl butyrate, which smells like apricot.
• It is closely related to pentyl butyrate and pentyl pentanoate, both of which are also present in fruits.
• It is closely related to pentyl butyrate and pentyl pentanoate, both of which are also present in fruits.
• It is an analogue of APINACA and 5F-APINACA where the pentyl chain has been replaced with fluorobenzyl.
• It is found naturally in the perennial flowering plant pentyl valerate are used as food additives because of their fruity flavors.
• The name is also used for the "'pentyl radical "', a pentyl group as an isolated molecule.
• The name is also used for the "'pentyl radical "', a pentyl group as an isolated molecule.
• The ester formed from 1-pentanol and acetic acid is amyl acetate ( also called pentyl acetate ), which smells like banana.
• In older literature, the common non-systematic name "'amyl "'was often used for the pentyl group.
• GS 4071 is cyclohexene based and has 3-pentyl ether, found to be optimal, instead of the glycerol as the side chain.
• Conversely, the name "'pentyl "'was used for several five-carbon branched alkyl groups, distinguished by various prefixes.
• NE-CHMIMO is the 1-cyclohexylmethyl ( instead of 1-pentyl ) analogue of the first-generation synthetic cannabinoid JWH-018.
• "' Pentyl hexanoate "'( C 5 H 11 COO . C 5 H 11 ) is an ester found in apple and pineapple fruits.
• In organic chemistry, "'pentyl "'is a five-carbon alkyl functional group ( substituent ) with chemical formula-C 5 H 11.
• Structurally it closely resembles cannabinoid compounds from patent WO 2003 / 035005 but with an indole core instead of indazole, and a simple pentyl chain on the indole 1-position.
• Their simulations suggested that drug resistance may arise from disruption of the binding process due to electrostatic attraction in charged neuraminidase pathways, in addition to disruption of Tamiflu's pentyl sidegroup.
• For example, when 3-pentanol is heated with aqueous HCl, the initially formed 3-pentyl carbocation rearranges to a statistical mixture of the 3-pentyl and 2-pentyl.
• For example, when 3-pentanol is heated with aqueous HCl, the initially formed 3-pentyl carbocation rearranges to a statistical mixture of the 3-pentyl and 2-pentyl.
• For example, when 3-pentanol is heated with aqueous HCl, the initially formed 3-pentyl carbocation rearranges to a statistical mixture of the 3-pentyl and 2-pentyl.