Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C8HCl3N2 |
| Molecular Weight | 231.466 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
ClC1=C(Cl)C(C#N)=C(Cl)C(=C1)C#N
InChI
InChIKey=GGTVBOHNZPIICP-UHFFFAOYSA-N
InChI=1S/C8HCl3N2/c9-6-1-4(2-12)7(10)5(3-13)8(6)11/h1H
| Molecular Formula | C8HCl3N2 |
| Molecular Weight | 231.466 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Transformation of the fungicide chlorothalonil by Fenton reagent. | 2002 Dec 18 |
|
| Study of chlorothalonil photodegradation in natural waters and in the presence of humic substances. | 2002 Sep |
|
| The persistence and degradation of chlorothalonil and chlorpyrifos in a cranberry bog. | 2003 Jan 1 |
|
| Degradation of chlorothalonil in irradiated water/sediment systems. | 2006 May 17 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 00:56:34 GMT 2023
by
admin
on
Sat Dec 16 00:56:34 GMT 2023
|
| Record UNII |
GDT158V252
|
| Record Status |
Validated (UNII)
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| Record Version |
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3015146
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23039-03-4
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GDT158V252
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DTXSID70177591
Created by
admin on Sat Dec 16 00:56:34 GMT 2023 , Edited by admin on Sat Dec 16 00:56:34 GMT 2023
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PRIMARY |