Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C8H16NO5P |
| Molecular Weight | 237.1901 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COP(=O)(OC)O\C(C)=C\C(=O)N(C)C
InChI
InChIKey=VEENJGZXVHKXNB-VOTSOKGWSA-N
InChI=1S/C8H16NO5P/c1-7(6-8(10)9(2)3)14-15(11,12-4)13-5/h6H,1-5H3/b7-6+
| Molecular Formula | C8H16NO5P |
| Molecular Weight | 237.1901 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Environmental impact on vascular development predicted by high-throughput screening. | 2011-11 |
|
| Activity profiles of 309 ToxCast™ chemicals evaluated across 292 biochemical targets. | 2011-03-28 |
|
| Esterase metabolism of cholinesterase inhibitors using rat liver in vitro. | 2011-03-15 |
|
| A comparative study on the relationship between various toxicological endpoints in Caenorhabditis elegans exposed to organophosphorus insecticides. | 2008 |
|
| The "intermediate syndrome" as critical sequelae of organophosphate poisoning: the first report of two cases in Thailand. | 2005-09 |
|
| Reactivation by various oximes of human erythrocyte acetylcholinesterase inhibited by different organophosphorus compounds. | 1996 |
|
| [On the plurifactorial determinism of the organophosphorous-induced teratogenesis on bird embryos; trials of protection by various compounds: oximes, hydroxamic acids and nicotinamide analogs (author's transl)]. | 1979 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 17:56:03 GMT 2025
by
admin
on
Mon Mar 31 17:56:03 GMT 2025
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| Record UNII |
B541I65WBL
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| Record Status |
Validated (UNII)
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| Record Version |
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EPA PESTICIDE CODE |
35201
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5371560
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1637
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m4367
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205-494-3
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141-66-2
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C000944
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C163647
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38658
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dicrotophos
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DICROTOPHOS
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DTXSID9023914
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B541I65WBL
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