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Cyclopentanone is common precursor to fragrances, especially those related to jasmine and jasmone. Examples include 2-pentyl- and 2-heptylcyclopentanone. [4] It is a versatile synthetic intermediate, being a precursor to cyclopentobarbital. [5] Cyclopentobarbital, a drug made from cyclopentanone
2-Cyclopentenone is the organic compound with the chemical formula (CH 2) 2 (CH) 2 CO. 2-Cyclopentenone contains two functional groups, a ketone and an alkene. It is a colorless liquid. Its isomer, 3-cyclopentenone is less commonly encountered.
Isomers with the molecular formula C 5 H 10 with CAS numbers C 5 H 10 is the molecular formula of 13 hydrocarbon isomers (represented by their CAS numbers on the chart). They can be divided into cycloalkanes and alkenes .
Download as PDF; Printable version; ... Chemical formula. C 5 H 10 O: Molar mass: 86.1323 g/mol Appearance Colorless liquid ... Cyclopentanone:
Cyclopentane (also called C pentane) [4] is a highly flammable alicyclic hydrocarbon with chemical formula C 5 H 10 and CAS number 287-92-3, consisting of a ring of five carbon atoms each bonded with two hydrogen atoms above and below the plane. It is a colorless liquid with a petrol-like odor.
SU-8 3000 series resists also use cyclopentanone for the primary solvent and are designed to be spun into thicker films ranging from 2 to 75 μm in a single coat. [14] SU-8 GLM2060 series of low-stress photoresist consist of epoxy GBL and silica formulation CTE 14. [15] SU-8 GCM3060 Series of GERSTELTEC conductive SU8 with nanoparticles of ...
2-[2-(4-Methyl-3-cyclohexen-1-yl)propyl]cyclopentanone (trade name by Givaudan: Nectaryl) is an organic compound belonging to the group of ketones and cycloalkanes. The compound is used as a fragrance .
Methylcyclopentane is an organic compound with the chemical formula CH 3 C 5 H 9. It is a colourless, flammable liquid with a faint odor. It is a colourless, flammable liquid with a faint odor. It is a component of the naphthene fraction of petroleum usually obtained as a mixture with cyclohexane .
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