Acifluorfen metabolite
Modify Date: 2025-08-25 17:05:04
Acifluorfen metabolite structure
|
Common Name | Acifluorfen metabolite | ||
|---|---|---|---|---|
| CAS Number | 50594-67-7 | Molecular Weight | 375.684 | |
| Density | 1.5±0.1 g/cm3 | Boiling Point | 392.3±42.0 °C at 760 mmHg | |
| Molecular Formula | C15H9ClF3NO5 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | 191.0±27.9 °C | |
Use of Acifluorfen metaboliteAcifluorfen-methyl is an inhibitor of the heme and chlorophyll biosynthetic enzyme protoporphyrinogen oxidase (Protox). Acifluorfen-methyl is a photobleaching herbicide[1]. |
| Name | acifluorfen-methyl |
|---|---|
| Synonym | More Synonyms |
| Description | Acifluorfen-methyl is an inhibitor of the heme and chlorophyll biosynthetic enzyme protoporphyrinogen oxidase (Protox). Acifluorfen-methyl is a photobleaching herbicide[1]. |
|---|---|
| Related Catalog | |
| References |
| Density | 1.5±0.1 g/cm3 |
|---|---|
| Boiling Point | 392.3±42.0 °C at 760 mmHg |
| Molecular Formula | C15H9ClF3NO5 |
| Molecular Weight | 375.684 |
| Flash Point | 191.0±27.9 °C |
| Exact Mass | 375.012146 |
| PSA | 81.35000 |
| LogP | 4.32 |
| Vapour Pressure | 0.0±0.9 mmHg at 25°C |
| Index of Refraction | 1.547 |
| HS Code | 2918990090 |
|---|
|
~27%
Acifluorfen met... CAS#:50594-67-7 |
| Literature: Rohm and Haas Company Patent: US4259510 A1, 1981 ; |
|
~82%
Acifluorfen met... CAS#:50594-67-7 |
| Literature: Rohm and Haas Company Patent: US4259510 A1, 1981 ; |
|
~%
Acifluorfen met... CAS#:50594-67-7 |
| Literature: Rohm and Haas Company Patent: US4031131 A1, 1977 ; |
![methyl 2-amino-5-[2-chloro-4-(trifluoromethyl)phenoxy]benzoate structure](https://image.chemsrc.com/caspic/226/58105-66-1.png)
CAS#:58105-66-1| HS Code | 2918990090 |
|---|---|
| Summary | 2918990090. other carboxylic acids with additional oxygen function and their anhydrides, halides, peroxides and peroxyacids; their halogenated, sulphonated, nitrated or nitrosated derivatives. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0% |
| Methyl 5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoate |
| 5-[2-Chloro-4-(trifluorométhyl)phénoxy]-2-nitrobenzoate de méthyle |
| 5-[2-Chloro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoic acid methyl ester |
| Acifluorfen methyl ester |
| Benzoic acid, 5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitro-, methyl ester |
| methyl 5-(2-chloro-α,α,α-trifluoro-p-tolyloxy)-2-nitrobenzoate |
| Methyl-5-[2-chlor-4-(trifluormethyl)phenoxy]-2-nitrobenzoat |
| Acifluorfen metabolite |