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1089014-47-0

1089014-47-0 Structure

1089014-47-0 Structure
IdentificationBack Directory
[Name]

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

1089014-47-0
[Synonyms]

9H-Purin-6-amine, 2-fluoro-N-(3-methoxyphenyl)-
[Molecular Formula]

C12H10FN5O
[MOL File]

1089014-47-0.mol
[Molecular Weight]

259.24
Chemical PropertiesBack Directory
[Melting point ]

195 °C
[Boiling point ]

612.4±65.0 °C(Predicted)
[density ]

1.474±0.06 g/cm3(Predicted)
[pka]

9.93±0.10(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]

Environment (GHS09)
GHS09
[Hazard statements ]

H411
Hazard InformationBack Directory
[Description]

A 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.
[Definition]

ChEBI: 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.
[Production Methods]

Anisiflupurin 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.
[Mechanism of action]

Inhibits cytokinin oxidase/dehydrogenase with plant growth regulators activity
[Pesticide Type]

Plant Growth Regulator
1089014-47-0 suppliers list
Company Name: HANGZHOU LEAP CHEM CO., LTD.
Tel: +86-571-87711850 +86-15355479329 , +86-15355479329
Website: www.leapchem.com
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