Cyazofamid information

Cyazofamid
Names
	IUPAC name 4-chloro-2-cyano-N,N-dimethyl-5-(4-methylphenyl)imidazole-1-sulfonamide
	Other names IKF 916
Identifiers
CAS Number	120116-88-3 ;
3D model (JSmol)	Interactive image;
Beilstein Reference	9064229
ChEBI	CHEBI:81841;
ChEMBL	ChEMBL1863429;
ChemSpider	8037772;
ECHA InfoCard	100.111.751
EC Number	601-671-8;
KEGG	C18573;
PubChem CID	9862076;
UNII	QJC4S2YQ4B;
CompTox Dashboard (EPA)	DTXSID9034492 ;
	InChI InChI=1S/C13H13ClN4O2S/c1-9-4-6-10(7-5-9)12-13(14)16-11(8-15)18(12)21(19,20)17(2)3/h4-7H,1-3H3 Key: YXKMMRDKEKCERS-UHFFFAOYSA-N;
	SMILES CC1=CC=C(C=C1)C2=C(N=C(N2S(=O)(=O)N(C)C)C#N)Cl;
Properties
Chemical formula	C13H13ClN4O2S
Molar mass	324.78 g·mol−1
Density	1.45 g/cm3
Melting point	152.7 °C
Solubility in water	0.107 mg/L (20 °C)
log P	3.2
Hazards
	GHS labelling:
Pictograms
Signal word	Warning
Hazard statements	H410
Precautionary statements	P273, P391, P501
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Cyazofamid is a fungicide that is highly-specific in controlling oomycete plant pathogens such as Phytophthora infestans, the organism which causes late blight in potato. Its mode of action is thought to involve binding to the Q_i center of Coenzyme Q – cytochrome c reductase.^[3]^[4]

Cyazofamid is most often sold under the brand name Ranman.^[5]

^ Pesticide Properties Database. "Cyazofamid". University of Hertfordshire.
^ PubChem Database. "Cyazofamid".
^ Mitani, Shigeru; Araki, Satoshi; Takii, Yasuko; Ohshima, Takeshi; Matsuo, Norifusa; Miyoshi, Hideto (October 2001). "The Biochemical Mode of Action of the Novel Selective Fungicide Cyazofamid: Specific Inhibition of Mitochondrial Complex III in Phythium spinosum". Pesticide Biochemistry and Physiology. 71 (2): 107–115. doi:10.1006/pest.2001.2569.
^ Mitani, Shigeru; Araki, Satoshi; Yamaguchi, Tomona; Takii, Yasuko; Ohshima, Takeshi; Matsuo, Norifusa (June 2001). "Antifungal Activity of the Novel Fungicide Cyazofamid against Phytophthora infestans and Other Plant Pathogenic Fungi in Vitro". Pesticide Biochemistry and Physiology. 70 (2): 92–99. doi:10.1006/pest.2001.2541.
^ "Fungicides". ISKBC – ISK Biosciences CORPORATION. Retrieved 2021-05-25.

[PPDB-1] Pesticide Properties Database. "Cyazofamid". University of Hertfordshire.

[PUBchem-2] PubChem Database. "Cyazofamid".

[3] Mitani, Shigeru; Araki, Satoshi; Takii, Yasuko; Ohshima, Takeshi; Matsuo, Norifusa; Miyoshi, Hideto (October 2001). "The Biochemical Mode of Action of the Novel Selective Fungicide Cyazofamid: Specific Inhibition of Mitochondrial Complex III in Phythium spinosum". Pesticide Biochemistry and Physiology. 71 (2): 107–115. doi:10.1006/pest.2001.2569.

[4] Mitani, Shigeru; Araki, Satoshi; Yamaguchi, Tomona; Takii, Yasuko; Ohshima, Takeshi; Matsuo, Norifusa (June 2001). "Antifungal Activity of the Novel Fungicide Cyazofamid against Phytophthora infestans and Other Plant Pathogenic Fungi in Vitro". Pesticide Biochemistry and Physiology. 70 (2): 92–99. doi:10.1006/pest.2001.2541.

[ISK-5] "Fungicides". ISKBC – ISK Biosciences CORPORATION. Retrieved 2021-05-25.

Cyazofamid information

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Cyazofamid

Fungicide

List of fungicides

Pseudoperonospora cubensis