3-methyl-2-pentanone
Structural formula | ||||||||||||||||
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Structural formula without stereochemistry | ||||||||||||||||
General | ||||||||||||||||
Surname | 3-methyl-2-pentanone | |||||||||||||||
other names |
Methyl sec- butyl ketone |
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Molecular formula | C 6 H 12 O | |||||||||||||||
External identifiers / databases | ||||||||||||||||
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properties | ||||||||||||||||
Molar mass | 100.16 g mol −1 | |||||||||||||||
Physical state |
liquid |
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density |
0.815 g cm −3 (25 ° C) |
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boiling point | ||||||||||||||||
Refractive index |
1.4 (20 ° C) |
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safety instructions | ||||||||||||||||
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As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . Refractive index: Na-D line , 20 ° C |
3-methyl-2-pentanone (also called methyl sec-butyl ketone ) is an organic chemical compound from the group of ketones . It is an isomer to 2-hexanone and 3-hexanone .
Extraction and presentation
It can be produced by oxidation of 3-methyl-2-pentanol .
Also possible is the representation by hydrogenation of 3-methyl-3-penten-2-one .
Stereochemistry
3-Methyl-2-pentanone is chiral and contains a stereocenter, so there are two stereoisomers , the ( R ) -3-methyl-2-pentanone and the ( S ) -3-methyl-2-pentanone. If 3-methyl-2-pentanone is mentioned without a prefix in this article or in the scientific literature, the racemate is always ( RS ) -3-methyl-2-pentanone, i.e. a 1: 1 mixture of ( R ) -3 -Methyl-2-pentanone and ( S ) -3-methyl-2-pentanone are meant.
use
3-methyl-2-pentanone can be used as an intermediate in the production of other chemical compounds (such as filberton ).
Individual evidence
- ↑ a b c d e data sheet 3-Methyl-2-pentanone, 99% from Sigma-Aldrich , accessed on November 6, 2014 ( PDF ).
- ↑ a b Google Patents: CN101597223B - Method for synthesizing filbertone - Google Patents , accessed January 12, 2019