212058-35-0

Upstream product

• 34182-03-1 (R)-5-(1-hydroxy-1-methylethyl)2-methylcyclohex-2-enone 
• 6610-21-5 6-methylcyclohex-2-en-1-one 
• 67-63-0 isopropyl alcohol 
• 116499-64-0 (R)-dihydrocarvone 
• 6485-40-1 (R)-Carvone 

Downstream Products

• 68524-96-9 (2S,5R)-5-(1-Hydroxy-1-methyl-ethyl)-2-methyl-2-pent-4-ynyl-cyclohexanone 
• 68568-09-2 (2S,5R)-5-(1-Hydroxy-1-methyl-ethyl)-2-methyl-2-pent-4-enyl-cyclohexanone 
• 68525-03-1 (2S,5R)-5-Isopropenyl-2-methyl-2-pent-4-ynyl-cyclohexanone 
• 68524-99-2 (2S,5R)-5-Isopropenyl-2-methyl-2-pent-4-enyl-cyclohexanone 

Relevant academic research and scientific papers

Buagafuran and preparation method of intermediate of buagafuran

The invention provides a preparation process route suitable for industrialized production of bulk drugs of buagafuran. The buagafuran is prepared through five steps of addition, cyclization, dehydration, carbonyl reduction and bridge ring formation. The t

Buagafuran Active Pharmaceutical Ingredient, Preparation Method and Application Thereof

A method suitable for large-scale production of buagafuran active pharmaceutical ingredient. A buagafuran active pharmaceutical ingredient (API) with a high purity prepared by the method includes an active ingredient of buagafuran, an impurity A, and an i

PHOTOCHEMISTRY OF 6-TRIFLUOROMETHYL-2-CYCLOHEXENONE

The photochemical behaviour of the title compound, newly synthesized from 2-trifluoromethylcyclohexanone by bromination/dehydrobromination sequence, is compared to that of 6-methyl-2-cyclohexenone.Both compounds behave similarly regarding photocyclodimerization and addition to 2-methylpropene.Higher yields of reduction (electron transfer) products from the trifluoromethyl- vs. the methyl enone are obtained in the irradiations in the presence of 2,3-dimethyl-2-butene or in propanol, respectively.