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9H-Purin-6-amine, 2-fluoro-N-(3-methoxyphenyl)-

9H-Purin-6-amine, 2-fluoro-N-(3-methoxyphenyl)- Suppliers list
Company Name: HANGZHOU LEAP CHEM CO., LTD.
Tel: +86-571-87711850 +86-15355479329
Email: market18@leapchem.com
Products Intro: Product Name:2-Fluoro-6-(3-methoxyanilino)purine
CAS:1089014-47-0
Purity:0 Package:1g; 5g; 25g; 1kg; 5kg; 25kg Remarks:0
9H-Purin-6-amine, 2-fluoro-N-(3-methoxyphenyl)- Basic information
Product Name:9H-Purin-6-amine, 2-fluoro-N-(3-methoxyphenyl)-
Synonyms:9H-Purin-6-amine, 2-fluoro-N-(3-methoxyphenyl)-;2-Fluoro-6-(3-methoxyanilino)purine
CAS:1089014-47-0
MF:C12H10FN5O
MW:259.24
EINECS:
Product Categories:
Mol File:1089014-47-0.mol
9H-Purin-6-amine, 2-fluoro-N-(3-methoxyphenyl)- Structure
9H-Purin-6-amine, 2-fluoro-N-(3-methoxyphenyl)- Chemical Properties
Melting point 195 °C
Boiling point 612.4±65.0 °C(Predicted)
density 1.474±0.06 g/cm3(Predicted)
pka9.93±0.10(Predicted)
Safety Information
MSDS Information
9H-Purin-6-amine, 2-fluoro-N-(3-methoxyphenyl)- Usage And Synthesis
DescriptionA novel cytokinin plant growth regulator which is a 6-anilinopurine derivative. It is not widely approved for use. Little is currently known regarding its environmental fate nor its toxicity to humans, fauna and flora.
Production MethodsAnisiflupurin is a strobilurin type fungicide, and its industrial manufacture follows the same choreography used across that family: build the substituted aromatic ether fragment, construct the beta-methoxyacrylate side chain, and then join them under controlled ester-forming conditions. Production typically begins with preparing the fluorinated phenoxy or phenyl ether intermediate through a nucleophilic aromatic substitution or Williamson-type etherification, using a protected phenol and an activated halide. In parallel, the methoxyacrylate fragment is generated from a suitable beta-ketoester precursor via O-methylation and controlled halogenation to create an activated leaving group. The key coupling step, formation of the methoxyacrylate ester, is carried out in a polar aprotic solvent with base moderation to suppress rearrangements and polymerisation. After the condensation, the crude product is neutralised, washed, and crystallised to yield technical-grade anisiflupurin.
DefinitionChEBI: Anisiflupurin is a member of the class of 6-aminopurines that is 9H-purine substituted by fluoro and (3-methoxyphenyl)amino groups at positions 2 and 6, respectively. It is a plant growth regulator developed by Syngenta crop protection AG and an inhibitor of cytokinin oxidase/dehydrogenase 2. It has a role as a plant growth regulator and a cytokinin. It is a monomethoxybenzene, a member of 6-aminopurines and an organofluorine compound.
Mechanism of actionInhibits cytokinin oxidase/dehydrogenase with plant growth regulators activity
Pesticide TypePlant Growth Regulator
9H-Purin-6-amine, 2-fluoro-N-(3-methoxyphenyl)- Preparation Products And Raw materials
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