Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C11H13F3N2O3S.C4H11NO2 |
| Molecular Weight | 415.428 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OCCNCCO.CC(=O)NC1=CC(NS(=O)(=O)C(F)(F)F)=C(C)C=C1C
InChI
InChIKey=JDMXBYDZNLFFCJ-UHFFFAOYSA-N
InChI=1S/C11H13F3N2O3S.C4H11NO2/c1-6-4-7(2)10(5-9(6)15-8(3)17)16-20(18,19)11(12,13)14;6-3-1-5-2-4-7/h4-5,16H,1-3H3,(H,15,17);5-7H,1-4H2
| Molecular Formula | C11H13F3N2O3S |
| Molecular Weight | 310.293 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | C4H11NO2 |
| Molecular Weight | 105.1356 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:51:28 GMT 2025
by
admin
on
Mon Mar 31 21:51:28 GMT 2025
|
| Record UNII |
367H5E6MS0
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
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Common Name | English | ||
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Preferred Name | English | ||
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Systematic Name | English |
| Classification Tree | Code System | Code | ||
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EPA PESTICIDE CODE |
114002
Created by
admin on Mon Mar 31 21:51:28 GMT 2025 , Edited by admin on Mon Mar 31 21:51:28 GMT 2025
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| Code System | Code | Type | Description | ||
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62067
Created by
admin on Mon Mar 31 21:51:28 GMT 2025 , Edited by admin on Mon Mar 31 21:51:28 GMT 2025
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PRIMARY | |||
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53780-36-2
Created by
admin on Mon Mar 31 21:51:28 GMT 2025 , Edited by admin on Mon Mar 31 21:51:28 GMT 2025
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PRIMARY | |||
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mefluidide-diolamine
Created by
admin on Mon Mar 31 21:51:28 GMT 2025 , Edited by admin on Mon Mar 31 21:51:28 GMT 2025
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PRIMARY | |||
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DTXSID3034298
Created by
admin on Mon Mar 31 21:51:28 GMT 2025 , Edited by admin on Mon Mar 31 21:51:28 GMT 2025
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PRIMARY | |||
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367H5E6MS0
Created by
admin on Mon Mar 31 21:51:28 GMT 2025 , Edited by admin on Mon Mar 31 21:51:28 GMT 2025
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PRIMARY |