form
solid
mp
208-210 °C (lit.)
functional group
chloro
SMILES string
ClC1=C(Cl)[C@@]2(Cl)C3C(C4C(c5ccccc35)[C@@]6(Cl)C(Cl)=C(Cl)[C@]4(Cl)C6(Cl)Cl)[C@]1(Cl)C2(Cl)Cl
InChI
1S/C20H8Cl12/c21-11-13(23)17(27)9-7(15(11,25)19(17,29)30)5-3-1-2-4-6(5)8-10(9)18(28)14(24)12(22)16(8,26)20(18,31)32/h1-4,7-10H/t7?,8?,9?,10?,15-,16+,17+,18-
InChI key
ULBZLTIPWBXWCY-QDCKJYKTSA-N
General description
Naphthalene-bis(hexachlorocyclopentadiene) adduct is precursor to substituted naphthalenes which are otherwise difficult to synthesize.
Application
Naphthalene-bis(hexachlorocyclopentadiene) adduct was used in the synthesis of:
- 2,3-diiodonaphthalene via iodination in methanesulfonic acid
- 2,3-dibromonapthalene via bromination
Reactant involved in iodination and retro Diels-alder reactions
Molecule studied for its pharmacological activity as a KSP inhibitor
Molecule studied for its pharmacological activity as a KSP inhibitor
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)