7213-64-1

Basic information

• Product Name: C₁₁H₁₀
• Synonyms: C₁₁H₁₀
• CAS NO: 7213-64-1
• Molecular Weight: 142.2
• Mol File: 7213-64-1.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: C₁₁H₁₀(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₁H₁₀(7213-64-1)
• EPA Substance Registry System: C₁₁H₁₀(7213-64-1)

Safety Data

• Hazardous Substances Data: 7213-64-1(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 7605-04-1 exo-2-benzonorbornenyl chloride 
• 4453-90-1 1,4-dihydro-1,4-methanonaphthalene 
• 70332-88-6 2,3-diaza-7,8-benzotricyclo<4.3.0.0^4,9>nona-2,7-diene 
• 67-63-0 isopropyl alcohol 
• 4453-90-1 1,4-dihydro-1,4-methanonaphthalene 
• 31351-14-1 exo-2-benzonorbornenyl mesylate 
• 75-65-0 tert-butyl alcohol 

Downstream Products

• 91-20-3 naphthalene 
• 4453-90-1 1,4-dihydro-1,4-methanonaphthalene 
• 3463-79-4 2,3-benzonorcaradiene 
• 90-12-0 1-Methylnaphthalene 
• 264-08-4 benzocycloheptatrien 
• 19770-38-8 spiro(cyclopropane-1,1'-<1H>-indene) 
• 4453-90-1 1,4-dihydro-1,4-methanonaphthalene 
• 24459-98-1 2-vinylindene 
• 80452-17-1 3a,7b-Dihydro-1H-cyclopenta[3,4]cyclobuta[1,2]benzene 
• 18511-42-7 (2aS,7aR)-7,7a-Dihydro-2aH-cyclobuta[a]indene 
• 3463-79-4 benzonorcaradiene 
• 74420-42-1 2-Phenyl-6,10b-dihydro-4H-2,3a,10c-triaza-cyclopenta[c]fluorene-1,3-dione 
• 78812-93-8 1-methyl-2-methoxy-1,4-dihydronaphthalene 

Relevant articles and documents

UNTERSUCHUNGEN ZUM THERMISCHEN UND PHOTOCHEMISCHEN VERHALTEN VON 8,9-DIAZA-4,5-BENZOTRICYCLO3,7>OCTA-4,8-DIEN

Die direkte Photolyse der Titelverbindung 1 verlaeuft erwartungsgemaess unter Stickstoffabspaltung zu 6.Dagegen fuehrt ihre Thermolyse und ihre sensibilisierte Bestrahlung zu den ueberraschenden Produkten 4 bzw. 8, deren spektroskopische Charakterisierung und moegliche Bildungsmechanismen diskutiert werden.

LIGHT-MEDIATED TRANSFORMATIONS OF OLEFINS INTO ALCOHOLS: REACTIONS OF HYDROXYL RADICALS WITH CYCLOALKENES

Reactions of hydroxyl radicals, generated by photodecomposition of hydrogen peroxide in acetonitrile, with a wide variety of cycloalkenes have been examined.The results show that the major reaction is the addition of hydroxyl radicals to the less substituted end of the double bond, furnishing the secondary alcohols.The reactivity pattern and the observed regio- and stereoselectivity clearly reveal that the steric parameters associated with the substrates play a dominant role in directing the addition reactions.More importantly, this study led to the development of a new methodology for the facile conversions of olefins essentially into secondary alcohols, and includes a few examples which demonstrate the potential of the method.

PHOTOCHEMISTRY OF BENZOTRICYCLO2,7>HEPTENE: SINGLET EXCITED STATE REACTIONS DERIVED FROM CYCLOPROPANE RING CLEAVAGE

Direct irradiation of the title hydrocarbon in cyclohexane affords 2-vinylindene and benzonorcaradiene as major primary photoproducts.Deuterium labeling is used to determine reaction mechanisms.