Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C7H14O2 |
| Molecular Weight | 130.1849 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCC(C)C(O)=O
InChI
InChIKey=CVKMFSAVYPAZTQ-UHFFFAOYSA-N
InChI=1S/C7H14O2/c1-3-4-5-6(2)7(8)9/h6H,3-5H2,1-2H3,(H,8,9)
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Characterisation of the most odour-active compounds of bone tainted dry-cured Iberian ham. | 2010-05 |
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| Natural organic compounds as alternative to methyl bromide for nematodes control. | 2008-11 |
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| Predicting olfactory receptor neuron responses from odorant structure. | 2007-05-04 |
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| Normal-phase chiral liquid chromatography-mass spectrometry of non-UV-active compounds: applications for pharmaceutically relevant racemates. | 2006-07-07 |
|
| Separation and conductimetric detection of C1-C7 aliphatic monocarboxylic acids and C1-C7 aliphatic monoamines on unfunctionized polymethacrylate resin columns. | 2004-06-11 |
|
| Application of polymethacrylate resin as stationary phase in liquid chromatography with UV detection for C1-C7 aliphatic monocarboxylic acids and C1-C7 aliphatic monoamines. | 2004-06-11 |
Patents
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| Classification Tree | Code System | Code | ||
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JECFA EVALUATION |
2-METHYLHEXANOIC ACID
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DTXSID9044241
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SUBSTANCE RECORD
