Naphthalene-bis(hexachlorocyclopentadiene) adduct

• Catalog No.: 184861
• CAS Number: 5696-92-4
• M. F.: C20H8Cl12
• M. W.: 673.71352

SYNONYMS

• Title: 萘-双(六氯环戊二烯)加合物
• IUPAC name: (1R,4S,7R,16S)-1,4,5,6,7,16,17,18,19,19,20,20-dodecachlorohexacyclo[14.2.1.1^4,^7.0^2,^1^5.0^3,^8.0^9,^1^4]icosa-5,9,11,13,17-pentaene
• IUPAC Traditional name: (1R,4S,7R,16S)-1,4,5,6,7,16,17,18,19,19,20,20-dodecachlorohexacyclo[14.2.1.1^4,^7.0^2,^1^5.0^3,^8.0^9,^1^4]icosa-5,9,11,13,17-pentaene
• Synonyms: DHA; NSC 122892

DATABASE IDS

• EC Number: 227-171-6
• CAS Number: 5696-92-4
• PubChem SID: 24850660
• MDL Number: MFCD00167975

PROPERTIES

• Empirical Formula (Hill Notation): C20H8Cl12
• Melting Point: 208-210 °C(lit.)
• Personal Protective Equipment: Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
• German water hazard class: 3

DETAILS

Description (English)

Packaging
500 g in poly bottle
Application
Precursor to substituted naphthalenes which are otherwise difficult to synthesize.1
Reactant involved in iodination and retro Diels-alder reactionsMolecule studied for its pharmacological activity as a KSP inhibitor

Description (简体中文)

包装
500 g in poly bottle
Application
Reactant involved in iodination and retro Diels-alder reactionsMolecule studied for its pharmacological activity as a KSP inhibitor
取代萘的前体，此类取代萘难以合成。1