Inabenfide
Inabenfide Basic information
- Product Name:
- Inabenfide
- Synonyms:
-
- SERITARD
- 4’-chloro-2’-(alpha-hydroxybenzyl)isonicotinanilide
- cgr-811
- n-(4-chloro-2-(hydroxyphenylmethyl)phenyl)-4-pyridinecarboxamid
- n-(4-chloro-2-(hydroxyphenylmethyl)phenyl)-4-pyridinecarboxamide
- INABENFIDE
- 4′-Chloro-2′-(α-hydroxybenzyl)isonicotinanilide
- N-[4-Chloro-2-(hydroxy-phenylmethyl)phenyl]pyridine-4-carboxamide
- CAS:
- 82211-24-3
- MF:
- C19H15ClN2O2
- MW:
- 338.79
- Product Categories:
-
- pyridine
- Mol File:
- 82211-24-3.mol
Inabenfide Chemical Properties
- Melting point:
- approximate 202℃ (dec.)
- Boiling point:
- 454.6±45.0 °C(Predicted)
- Density
- 1.2238 (rough estimate)
- refractive index
- 1.5400 (estimate)
- storage temp.
- 0-6°C
- pka
- 10.77±0.70(Predicted)
- BRN
- 7042400
- CAS DataBase Reference
- 82211-24-3(CAS DataBase Reference)
Inabenfide Usage And Synthesis
Application
Inabenfide (N-[4-chloro-2-(hydroxybenzyl)phenyl]pyridine-4-carboxamide) is a plant growth retardant that inhibits gibberellin synthesis in rice plants, exhibiting strong selective lodging resistance. After application, the number of grains per panicle decreases, but the grain maturity rate increases, leading to an increase in actual yield. Therefore, inabenfide is widely used in rice production.
Definition
ChEBI: Inabenfide is a diarylmethane.
Metabolic pathway
In rats, inabenfide is mainly hydroxylated on the phenyl ring which is not substituted by a chlorine atom through epoxidation. Oxidation of the benzyl alcohol gives benzophenone. The other hydroxylation is the substitution of the chlorine with hydroxyl of the other phenyl ring possessing a chlorine atom. Also, hydrolysis of the amide bond resulting in the corresponding aniline and N-oxidation of the pyridine nitrogen can be observed.
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Inabenfide(82211-24-3)Related Product Information
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- Phenylhydrazine
- Formamide
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- CHLOROPHOSPHONAZO III
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- Epichlorohydrin
- Benzyltriphenylphosphonium chloride
- PHENYL VALERATE
- Trinexapac-ethyl
- N,N-Dimethylformamide
- Difluorochloromethane
- Chloroacetic acid
- N-phenyl isonicotinamide
- 2-AMINO-5-CHLOROBENZYL ALCOHOL
- 2-amino-5-chloro-diphenyl methanol
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- 2-AMINOBENZHYDROL