| Identification | Back Directory | [Name]
DIHYDROHEPTACHLOR | [CAS]
14168-01-5 | [Synonyms]
DIHYDROHEPTACHLOR
Heptachlor-beta-dihydro
2-exo-4,5,6,7,8,8-Heptachlor-4,7-methano-3a,4,7,7a-tetrahydro-indan, β-Dihydro-heptachlor
(2,3a,4,7,7a)-2,4,5,6,7,8,8-heptachloro-2,3,3a,4,7,7a-hexahydro-4,7- methano-1H-indene
4,7-Methano-1H-indene, 2,4,5,6,7,8,8-heptachloro-2,3,3a,4,7,7a-hexahydro-, (2α,3aα,4β,7β,7aα)- | [Molecular Formula]
C10H7Cl7 | [MOL File]
14168-01-5.mol | [Molecular Weight]
375.33 |
| Chemical Properties | Back Directory | [Melting point ]
135 °C(Solv: carbon tetrachloride (56-23-5)) | [Boiling point ]
460.86°C (rough estimate) | [density ]
1.6255 (rough estimate) | [refractive index ]
1.6200 (estimate) | [EPA Substance Registry System]
4,7-Methano-1H-indene, 2,4,5,6,7,8,8-heptachloro-2,3,3a,4,7,7a-hexahydro-, (2.alpha.,3a.alpha.,4.beta.,7.beta.,7a.alpha.)- (14168-01-5) |
| Hazard Information | Back Directory | [Production Methods]
The commercial production process of beta-dihydroheptachlor is not available in open literature. However, based on its structure, production would start from a chlorinated norbornene type precursor, undergo controlled addition and rearrangement reactions to generate the bicyclic chlorinated framework, and then a stereochemical conversion process would be undertaken to obtain the beta dihydro isomer. | [Mechanism of action]
Central nervous system stimulant. GABA-gated chloride channel antagonist. Also stomach and contact toxin | [Pesticide Type]
Insecticide |
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