60968-01-6

Usage

InChI:InChI=1/C18H14/c1-2-7-15-12-18-16(11-14(15)6-1)10-9-13-5-3-4-8-17(13)18/h1-2,4,6-12H,3,5H2

Upstream product

• 57652-74-1 3,4-dihydrobenzanthracen-1(2H)-one 
• 60968-00-5 (+/-)-1-hydroxy-1,2,3,4-tetrahydrobenzanthracene 

Downstream Products

• 90997-20-9 (-)-(1R,2R)-trans-2-bromo-1-menthyloxyacetoxy-1,2,3,4-tetrahydrobenzanthracene 
• 91050-74-7 (+)-(1S,2S)-trans-2-bromo-1-menthyloxyacetoxy-1,2,3,4-tetrahydrobenzanthracene 
• 90997-21-0 (S)-3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid (1R,2R)-2,4-dibromo-1,2,3,4-tetrahydro-benzo[a]anthracen-1-yl ester 
• 90997-22-1 (-)-(2S)-2-hydroxy-1,2,3,4-tetrahydrobenzanthracene 
• 80522-78-7 (+)-(1R,2R)-trans-2-bromo-1-<2-methoxy-2-phenyl-2-trifluoromethylacetoxy>-1,2,3,4-tetrahydrobenzanthracene 
• 80522-84-5 (-)-(1S,2S)-trans-2-bromo-1-<2-methoxy-2-phenyl-2-trifluoromethylacetoxy>-1,2,3,4-tetrahydrobenzanthracene 
• 89618-16-6 (+)-(1R,2S)-1,2-Epoxy-1,2,3,4-tetrahydrobenzanthracene 
• 90997-19-6 (+/-)-trans-2-bromo-1-hydroxy-1,2,3,4-tetrahydrobenzanthracene 
• 60968-03-8 1,2-Dihydroxy-1,2,3,4-tetrahydrobenzanthracene 

Relevant academic research and scientific papers

Acid catalysed reaction of indanones, tetralones and benzosuberone with neopentyl glycol and other alkanediols under forced conditions

Upon reaction with an excess of 2,2-dimethylpropane-1,3-diol (neopentyl glycol, NPG) under acid catalysis, indanones and tetralones yield indenes and dihydronaphthalenes, respectively. The reaction can also be carried out with butane-1,3-diol.

Synthesis and Spontaneous Racemization of Benzanthracene 1,2-Oxide

Benzanthracene 1,2-oxide (1,2-epoxy-1,2-dihydrobenzanthracene), a minor metabolite of benzanthracene in hepatic systems, has been synthesized both from racemic precursors and from separated diastereoisomeric bromohydrin esters whose absolute ster