| Company Name: |
InvivoChem |
| Tel: |
13549236410 |
| Email: |
sales@invivochem.cn |
3-Pyridinecarboxylic acid, 2-amino-6-methyl-, (4-phenoxyphenyl)methyl ester manufacturers
- Aminopyrifen
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- $2670.00
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2026-06-15
- CAS:1531626-08-0
- Purity: 99.34%
- Supply Ability: 10g
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| | 3-Pyridinecarboxylic acid, 2-amino-6-methyl-, (4-phenoxyphenyl)methyl ester Basic information |
| | 3-Pyridinecarboxylic acid, 2-amino-6-methyl-, (4-phenoxyphenyl)methyl ester Chemical Properties |
| Boiling point | 485.6±45.0 °C(Predicted) | | density | 1.236±0.06 g/cm3(Predicted) | | pka | 4.66±0.50(Predicted) |
| | 3-Pyridinecarboxylic acid, 2-amino-6-methyl-, (4-phenoxyphenyl)methyl ester Usage And Synthesis |
| Description | Aminopyrifen is a pyridine fungicide. Currently data relating to its environmental fate, ecotoxicology and human health effects is scant. | | Production Methods | Aminopyrifen is produced through a modular heterocycle-assembly route characteristic of modern pyridazinone-based herbicides. Commercial manufacture begins with construction of the substituted pyridazinone core, typically formed by condensing a di-carbonyl precursor with an appropriate hydrazine derivative under conditions that tightly control ring closure and prevent over reaction of the sensitive heterocycle. In parallel, the fluorinated and chlorinated aromatic fragment that defines aminopyrifen’s herbicidal profile is prepared using established halogenation and nucleophilic-substitution chemistry chosen to preserve the integrity of the heteroaromatic ring. These two advanced intermediates are then joined through a selective coupling step, often an amide-forming or heteroaryl-aryl bond forming reaction, to assemble the full aminopyrifen scaffold without degrading the halogenated moieties. | | Mechanism of action | Inhibits the GWT-1 protein in glycosylphosphatidylinositol-anchor biosynthesis | | Pesticide Type | Fungicide |
| | 3-Pyridinecarboxylic acid, 2-amino-6-methyl-, (4-phenoxyphenyl)methyl ester Preparation Products And Raw materials |
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