| Identification | Back Directory | [Name]
DIFLUMETORIM | [CAS]
130339-07-0 | [Synonyms]
ubf-002
DIFLUMETORIM
Diflumetorim [iso]
DIFLUMETORIM STANDARD
diflumetorim (bsi, pa iso)
5-Chloro-N-{1-[4-(difluoromethoxy)Phenyl]Propyl}-6-methyl-4-pyrimidinamine
4-Pyrimidinamine, 5-chloro-N-[1-[4-(difluoromethoxy)phenyl]propyl]-6-methyl- | [Molecular Formula]
C15H16ClF2N3O | [MDL Number]
MFCD03427396 | [MOL File]
130339-07-0.mol | [Molecular Weight]
327.76 |
| Chemical Properties | Back Directory | [Melting point ]
46～50℃ | [Boiling point ]
431.8±45.0 °C(Predicted) | [density ]
1.293±0.06 g/cm3(Predicted) | [pka]
4.06±0.10(Predicted) | [Henry's Law Constant]
3.1×102 mol/(m3Pa) at 25℃, Duchowicz et al. (2020) |
| Hazard Information | Back Directory | [Uses]
Diflumetorim is used in pesticide formulations functioning as a fungicide. | [Definition]
ChEBI: 5-chloro-N-{1-[4-(difluoromethoxy)phenyl]propyl}-6-methylpyrimidin-4-amine is a member of the class of aminopyrimidines that is 5-chloro-6-methylpyrimidin-4-amine in which one of the amino hydrogens is replaced by a 1-[4-(difluoromethoxy)phenyl]propyl group. It is an aminopyrimidine, an organochlorine compound, an organofluorine compound, an aromatic ether and a secondary amino compound. | [Production Methods]
The production of diflumetorim begins with the formation of a pyrimidinamine core, which is selectively chlorinated at the 5-position and methylated at the 6-position. A key step involves nucleophilic substitution to attach a 4-(difluoromethoxy)phenylpropyl side chain to the nitrogen atom, enhancing lipophilicity and systemic activity. The resulting compound, 5-chloro-N-[1-[4-(difluoromethoxy)phenyl]propyl]-6-methylpyrimidin-4-amine, is purified and formulated. | [Mechanism of action]
Protectant and curative activity, inhibition of complex I NADH Oxido-reductase. | [Pesticide Type]
Fungicide |
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| Company Name: |
Carbosynth
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+86 512 6260 5585 |
| Website: |
www.carbosynth.com |
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