Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C17H24O3 |
| Molecular Weight | 276.3707 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=C(CC=C)C(=O)CC1OC(=O)C2C(C)(C)C2(C)C
InChI
InChIKey=MIZYPRIEDMSCAC-UHFFFAOYSA-N
InChI=1S/C17H24O3/c1-7-8-11-10(2)13(9-12(11)18)20-15(19)14-16(3,4)17(14,5)6/h7,13-14H,1,8-9H2,2-6H3
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Enantiomeric separation of chiral pesticides by high performance liquid chromatography on cellulose tris-3,5-dimethyl carbamate stationary phase under reversed phase conditions. | 2007-02 |
|
| Preparation of tetramethylcyclopropanecarboxylic-14C acid and insecticidal terallethrin-14C from it. | 1981-08 |
Patents
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Preferred Name | English | ||
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Code | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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6THJ337EJ9
Created by
admin on Mon Mar 31 22:52:13 GMT 2025 , Edited by admin on Mon Mar 31 22:52:13 GMT 2025
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PRIMARY | |||
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C180828
Created by
admin on Mon Mar 31 22:52:13 GMT 2025 , Edited by admin on Mon Mar 31 22:52:13 GMT 2025
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PRIMARY | |||
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DTXSID8057984
Created by
admin on Mon Mar 31 22:52:13 GMT 2025 , Edited by admin on Mon Mar 31 22:52:13 GMT 2025
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PRIMARY | |||
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239-651-2
Created by
admin on Mon Mar 31 22:52:13 GMT 2025 , Edited by admin on Mon Mar 31 22:52:13 GMT 2025
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PRIMARY | |||
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15589-31-8
Created by
admin on Mon Mar 31 22:52:13 GMT 2025 , Edited by admin on Mon Mar 31 22:52:13 GMT 2025
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PRIMARY | |||
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33855-51-5
Created by
admin on Mon Mar 31 22:52:13 GMT 2025 , Edited by admin on Mon Mar 31 22:52:13 GMT 2025
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SUPERSEDED | |||
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27409
Created by
admin on Mon Mar 31 22:52:13 GMT 2025 , Edited by admin on Mon Mar 31 22:52:13 GMT 2025
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PRIMARY | |||
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terallethrin
Created by
admin on Mon Mar 31 22:52:13 GMT 2025 , Edited by admin on Mon Mar 31 22:52:13 GMT 2025
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PRIMARY |
SUBSTANCE RECORD