Fenpropimorph

Fenpropimorph
Names
	IUPAC name cis-2,6-Dimethyl-4-{2-methyl-3-[4-(2-methyl-2-propanyl)phenyl]propyl}morpholine or (2R,6S)-4-[3-(4-tert-butylphenyl)-2-methylpropyl]-2,6-dimethylmorpholine
	Other names BAS 42100F; Corbel; Forbel 750; Mistral
Identifiers
CAS Number	67564-91-4 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:50145;
ChEMBL	ChEMBL372700;
ChemSpider	84290;
ECHA InfoCard	100.060.636
PubChem CID	93365;
CompTox Dashboard (EPA)	DTXSID901045927 DTXSID4034601, DTXSID901045927 ;
	InChI InChI=1S/C20H33NO/c1-15(12-21-13-16(2)22-17(3)14-21)11-18-7-9-19(10-8-18)20(4,5)6/h7-10,15-17H,11-14H2,1-6H3/t15?,16-,17+ Key: RYAUSSKQMZRMAI-ALOPSCKCSA-N; InChI=1/C20H33NO/c1-15(12-21-13-16(2)22-17(3)14-21)11-18-7-9-19(10-8-18)20(4,5)6/h7-10,15-17H,11-14H2,1-6H3/t15?,16-,17+ Key: RYAUSSKQMZRMAI-ALOPSCKCBN;
	SMILES O2[C@H](CN(CC(C)Cc1ccc(cc1)C(C)(C)C)C[C@H]2C)C;
Properties
Chemical formula	C20H33NO
Molar mass	303.490 g·mol−1
Appearance	Colorless liquid
Boiling point	120 °C (248 °F; 393 K) (0.067 mbar)
Solubility in water	4.3 mg/L (20 °C)
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Fenpropimorph is a morpholine-derived fungicide used in agriculture, primarily on cereal crops such as wheat.^[1] It works by inhibiting the sterol pathway of the fungus while plants are unaffected ^[2]

External links

Fenpropimorph, alanwood.net
Fenpropimorph in the Pesticide Properties DataBase (PPDB)

References

^ ^a ^b ^c ^d Fenpropimorph, Food and Agriculture Organization of the United Nations
^ [1] Antifungal Agents: Chemotherapeutic Targets and Immunologic Strategies, NAFSIKA H. GEORGOPAPADAKOU AND THOMAS J. WALSH, PMID 8834867

This article about a heterocyclic compound is a stub. You can help Wikipedia by expanding it.

[FAO-1] Fenpropimorph, Food and Agriculture Organization of the United Nations

[PUB-2] [1] Antifungal Agents: Chemotherapeutic Targets and Immunologic Strategies, NAFSIKA H. GEORGOPAPADAKOU AND THOMAS J. WALSH, PMID 8834867

[1]

[2]