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CAS 3232-62-0

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2,3-Di-2-propen-1-yl 1,4,5,6,7,7-hexachlorobicyclo[2.2.1]hept-5-ene-2,3-dicarboxylate

Description:
2,3-Di-2-propen-1-yl 1,4,5,6,7,7-hexachlorobicyclo[2.2.1]hept-5-ene-2,3-dicarboxylate, with CAS number 3232-62-0, is a synthetic organic compound characterized by its complex bicyclic structure and multiple chlorinated substituents. This compound features a bicyclo[2.2.1]heptene core, which is heavily chlorinated, contributing to its stability and potential biological activity. The presence of two propenyl groups indicates that it can undergo various chemical reactions, such as polymerization. The dicarboxylate functional groups suggest that it may exhibit acidic properties and could participate in esterification or other reactions involving carboxylic acids. Due to its chlorinated nature, this compound may also possess significant environmental persistence and potential toxicity, which is a consideration in its handling and application. Overall, its unique structure and functional groups make it of interest in fields such as organic synthesis, materials science, and potentially in agrochemical applications.
Formula:C15H12Cl6O4
InChI:InChI=1S/C15H12Cl6O4/c1-3-5-24-11(22)7-8(12(23)25-6-4-2)14(19)10(17)9(16)13(7,18)15(14,20)21/h3-4,7-8H,1-2,5-6H2
InChI key:InChIKey=CJKWEXMFQPNNTL-UHFFFAOYSA-N
SMILES:ClC12C(C(OCC=C)=O)C(C(OCC=C)=O)C(Cl)(C1(Cl)Cl)C(Cl)=C2Cl
Synonyms:
  • Diallyl chlorendate
  • Bicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic acid, 1,4,5,6,7,7-hexachloro-, 2,3-di-2-propen-1-yl ester
  • 5-Norbornene-2,3-dicarboxylic acid, 1,4,5,6,7,7-hexachloro-, diallyl ester
  • Bicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic acid, 1,4,5,6,7,7-hexachloro-, di-2-propenyl ester
  • 2,3-Di-2-propen-1-yl 1,4,5,6,7,7-hexachlorobicyclo[2.2.1]hept-5-ene-2,3-dicarboxylate
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