Binapacryl

Binapacryl^[1]

Names
IUPAC name (RS)-(2-Butan-2-yl-4,6-dinitrophenyl) 3-methylbut-2-enoate
Other names Dapacryl; Morocide; Morrocid; Acricid; Endosan; Ambox; Dinoseb methacrylate
Identifiers
CAS Registry Number	485-31-4 N
ChEBI	CHEBI:82153 N
ChemSpider	9817 Y
InChI InChI=1S/C15H18N2O6/c1-5-10(4)12-7-11(16(19)20)8-13(17(21)22)15(12)23-14(18)6-9(2)3/h6-8,10H,5H2,1-4H3 Y Key: ZRDUSMYWDRPZRM-UHFFFAOYSA-N Y InChI=1/C15H18N2O6/c1-5-10(4)12-7-11(16(19)20)8-13(17(21)22)15(12)23-14(18)6-9(2)3/h6-8,10H,5H2,1-4H3 Key: ZRDUSMYWDRPZRM-UHFFFAOYAH
Jmol-3D images	Image
KEGG	C19022 N
PubChem	10234
SMILES O=C(Oc1c(cc(cc1C(C)CC)[N+]([O-])=O)[N+]([O-])=O)\C=C(/C)C
UNII	4X685BB13A Y
Properties
Molecular formula	C15H18N2O6
Molar mass	322.31 g·mol−1
Density	1.2 g/cm3
Melting point	66 to 67 °C (151 to 153 °F; 339 to 340 K)
Solubility in water	Insoluble
Hazards
R-phrases	R21/22 R50/53 R61
S-phrases	S45 S53 S60 S61
Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
N verify (what is: Y/N?)
Infobox references

Binapacryl is an miticide and fungicide.^[2] Chemically, it is an ester derivative of dinoseb. Although binapacryl has low toxicity itself, it is readily metabolized to form dinoseb, which is toxic.^[1]

International trade in binapacryl is regulated by the Rotterdam Convention.

References