| Company Name: |
SPIRO PHARMA |
| Tel: |
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| Email: |
eric_feng1954@126.com |
Naxillin manufacturers
- Naxillin
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2026-07-29
- CAS:301176-96-5
- Purity: 99.22%
- Supply Ability: 10g
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| | Naxillin Basic information |
| Product Name: | Naxillin | | Synonyms: | Naxillin;[(E)-[5-[3-(trifluoromethyl)phenyl]furan-2-yl]methylideneamino]thiourea;Hydrazinecarbothioamide, 2-[[5-[3-(trifluoromethyl)phenyl]-2-furanyl]methylene]- | | CAS: | 301176-96-5 | | MF: | C13H10F3N3OS | | MW: | 313.3 | | EINECS: | | | Product Categories: | | | Mol File: | 301176-96-5.mol |  |
| | Naxillin Chemical Properties |
| Boiling point | 427.370±55.00 °C(Press: 760.00 Torr)(predicted) | | density | 1.422±0.14 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted) | | pka | 11.257±0.70(predicted) |
| | Naxillin Usage And Synthesis |
| Description | Naxillin is the first non-auxin-like molecule that promotes root branching. It acts as a specific modulator of lateral root development. | | Uses | Naxillin is a non-auxin-like molecule, which can promote the lateral root branching in the basal meristem of the root, through the conversion of the auxin precursor indole-3-butyric acid (IBA) to the active auxin indole-3-acetic acid (IAA)[1]. | | References | [1] De Rybel B, et al., A role for the root cap in root branching revealed by the non-auxin probe naxillin. Nat Chem Biol. 2012 Sep;8(9):798-805. DOI:10.1038/nchembio.1044 |
| | Naxillin Preparation Products And Raw materials |
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