Acibenzolar-S-methyl

Acibenzolar-S-methyl^[1]
Skeletal formula of acibenzolar-S-methyl
Names
	IUPAC name S-Methyl 1,2,3-benzothiadiazole-7-carbothioate[citation needed]
	Systematic IUPAC name 1,2,3-Benzothiadiazol-7-yl(methylsulfanyl)methanone[citation needed]
Identifiers
CAS Number	135158-54-2 ;
3D model (JSmol)	Interactive image; Interactive image;
ChEBI	CHEBI:73178 ;
ChEMBL	ChEMBL425055 ;
ChemSpider	77928 ;
ECHA InfoCard	100.101.876
EC Number	420-050-0;
MeSH	S-methyl+benzo(1,2,3)thiadiazole-7-carbothioate
PubChem CID	86412;
UNII	BCW6119347 ;
CompTox Dashboard (EPA)	DTXSID1032519 ;
	InChI InChI=1S/C8H6N2OS2/c1-12-8(11)5-3-2-4-6-7(5)13-10-9-6/h2-4H,1H3 Key: UELITFHSCLAHKR-UHFFFAOYSA-N ; InChI=1/C8H6N2OS2/c1-12-8(11)5-3-2-4-6-7(5)13-10-9-6/h2-4H,1H3 Key: UELITFHSCLAHKR-UHFFFAOYAA;
	SMILES CSC(=O)c1cccc2nnsc12; CSC(=O)C1=C2SN=NC2=CC=C1;
Properties
Chemical formula	C8H6N2OS2
Molar mass	210.27 g·mol−1
Appearance	Pale, light orange, opaque crystals
Melting point	133 °C (271 °F; 406 K)
Solubility in water	7.7 mg dm−3
log P	2.741
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Acibenzolar-S-methyl is a fungicide that works by activating a plant's own defense system by increasing the transcription of W-box controlled genes such as CAD1, NPR1 and PR2. It is a methyl derivative of acibenzolar.

References

^ EPA Fact Sheet: Acibenzolar-S-Methyl, August 11, 2000.

External links

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

[EPA-1] EPA Fact Sheet: Acibenzolar-S-Methyl, August 11, 2000.

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