Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C10H16O2 |
| Molecular Weight | 168.2328 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)=C[C@H]1[C@@H](C(O)=O)C1(C)C
InChI
InChIKey=XLOPRKKSAJMMEW-YUMQZZPRSA-N
InChI=1S/C10H16O2/c1-6(2)5-7-8(9(11)12)10(7,3)4/h5,7-8H,1-4H3,(H,11,12)/t7-,8-/m0/s1
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Characteristics and function of Alcaligenes sp. NBRC 14130 esterase catalysing the stereo-selective hydrolysis of ethyl chrysanthemate. | 2010-04 |
|
| The racemate cage. Influence of p(1),n(1) salt occurrence on enantiomer separation processes. The case of trans-chrysanthemic acid. | 2007-07-14 |
|
| p1,n1 salts: Self-assembled supramolecular structures sequestering racemates. Diastereomeric separation and enantiomeric enrichment of trans-chrysanthemic acid. | 2006-11-04 |
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220-908-2
Created by
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2935-23-1
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m3525
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admin on Mon Mar 31 21:38:45 GMT 2025 , Edited by admin on Mon Mar 31 21:38:45 GMT 2025
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39103
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1J3B3RQ0Q8
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admin on Mon Mar 31 21:38:45 GMT 2025 , Edited by admin on Mon Mar 31 21:38:45 GMT 2025
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SUBSTANCE RECORD
