Chemistry:Prodiamine
From HandWiki
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| Preferred IUPAC name
2,6-Dinitro-N1,N1-dipropyl-4-(trifluoromethyl)benzene-1,3-diamine | |
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3D model (JSmol)
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| Properties | |
| C13H17F3N4O4 | |
| Molar mass | 350.298 g·mol−1 |
| Melting point | 124–125 °C (255–257 °F; 397–398 K)[1] |
| Hazards | |
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| GHS Signal word | Warning |
| H332, H410 | |
| P261, P271, P273, P304+312, P304+340, P312, P391, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
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Tracking categories (test):
Prodiamine is a preemergent herbicide of the dinitroaniline class. Prodiamine is used with crops such as soybeans, alfalfa, cotton, and ornamental crops. Prodiamine inhibits the formation of microtubules.[2]
Prodiamine was developed by Sandoz AG and marketed beginning in 1987.[3]
Prodiamine can be obtained starting from 2,4-dichlorobenzotrifluoride.[4]
References
- ↑ Endeshaw, Molla M; Li, Catherine; Leon, Jessica de; Yao, Ni; Latibeaudiere, Kirk; Premalatha, Kokku; Morrissette, Naomi; Werbovetz, Karl A (2010). "Synthesis and evaluation of oryzalin analogs against Toxoplasma gondii". Bioorganic & Medicinal Chemistry Letters 20 (17): 5179. doi:10.1016/j.bmcl.2010.07.003. PMID 20675138.
- ↑ "Herbicide Mode-Of-Action Summary". Purdue University. http://www.extension.purdue.edu/extmedia/ws/ws-23-w.html.
- ↑ Entry on Prodiamin. at: Römpp Online. Georg Thieme Verlag, retrieved 8 June 2020.
- ↑ Thomas A. Unger (1996). Pesticide Synthesis Handbook. p. 877. ISBN 978-0-8155-1401-5.
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