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 Number	485-31-4^N
3D model (Jmol)	Interactive image
ChEBI	CHEBI:82153^N
ChemSpider	9817^Y
ECHA InfoCard	100.006.921
KEGG	C19022^N
PubChem	10234
UNII	4X685BB13A^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
SMILES O=C(Oc1c(cc(cc1C(C)CC)[N+]([O-])=O)[N+]([O-])=O)\C=C(/C)C
Properties
Chemical formula	C₁₅H₁₈N₂O₆
Molar mass	322.32 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 otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is ^YN ?)
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

1 2 Datasheet from International Programme on Chemical Safety
↑ Binapacryl at alanwood.net

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