125013-86-7

Basic information

• Product Name: (1R,4S,4aR,8aS)-6-Bromo-7-chloro-1,4,4a,5,6,8a-hexahydro-1,4-methano-naphthalene
• Synonyms: (1R,4S,4aR,8aS)-6-Bromo-7-chloro-1,4,4a,5,6,8a-hexahydro-1,4-methano-naphthalene
• CAS NO: 125013-86-7
• Molecular Weight: 259.573
• Mol File: 125013-86-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (1R,4S,4aR,8aS)-6-Bromo-7-chloro-1,4,4a,5,6,8a-hexahydro-1,4-methano-naphthalene(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,4S,4aR,8aS)-6-Bromo-7-chloro-1,4,4a,5,6,8a-hexahydro-1,4-methano-naphthalene(125013-86-7)
• EPA Substance Registry System: (1R,4S,4aR,8aS)-6-Bromo-7-chloro-1,4,4a,5,6,8a-hexahydro-1,4-methano-naphthalene(125013-86-7)

Safety Data

• Hazardous Substances Data: 125013-86-7(Hazardous Substances Data)

Upstream product

• 124-48-1 chlorodibromomethane 
• 1755-01-7 endo-Dicyclopentadien 

Relevant articles and documents

SYNTHESIS OF ADDUCTS OF DIHALOGENOCARBENES WITH THE DIMERS OF CYCLOPENTADIENE AND SPIROHEPTA-4,6-DIENE AND THEIR THERMAL TRANSFORMATIONS

It was found that dichloro-, dibromo-, bromochloro-, and bromofluorocarbenes react with the cyclopentadiene dimer (tricyclo2,6>deca-3,8-diene) and the spirohepta-4,6-diene dimer cyclopropanespiro-5-(tricyclo2,6>deca-3,8-diene)-10-spirocyclopropane with the exclusive formation of the adducts at the double bond of the cyclopentene fragment, i.e., 4,4-dihalogenotetracyclo2,7.03,5>undec-5-enes and cyclopropanespiro-6-(4,4-dihalogenotetracyclo2,7.03,5>undec-9-ene)-11-spirocyclopropanes respectively.When the adducts of the carbenes are heated with the cyclopentadiene dimer, they undergo thermal isomerization with opening of the three-membered ring, leading to 4,5-dihalogenotricyclo2,7>undeca-3,9-dienes.The adducts of the carbenes with the spirohepta-4,6-diene dimer undergo the reverse Diels-Alder reaction when heated with the formation of cyclopropanespiro-5-(tricyclo2,6>deca-3,8-diene)-10-spirocyclopropane and 3-(2-halogenoethyl)halogenobenzenes.