I agree Our site saves small pieces of text information (cookies) on your device in order to deliver better content and for statistical purposes. You can disable the usage of cookies by changing the settings of your browser. By browsing our website without changing the browser settings you grant us permission to store that information on your device.
It is used as a nitisinone intermediate.
Biswanath Das,; Ponnaboina Thirupathi,; K. Ravinder Reddy,; B. Ravikanth,; Lingaiah Nagarapu.1,3-Cyclohexanedione, 97+%, may cont. up to 1% NaCl. Catalysis Communications.2007 , 8 (3),535-538.
authors. title . Journal name. year of publication , volume issue , pg no.
For procedures for the conversion to the mono- and bis-silyl enol ethers, using HMDS/ imidazole and LDA/ TMS chloride respectively, see: Synthesis, 431 (1977).
Reacts with primary amines to give ß-amino enones, which can be aromatized to m-amino-phenols by oxidation with Hg(OAc)2: Synthesis, 471 (1982).
Gefahrenhinweise (EU): H302
Harmful if swallowed.
Wash thoroughly after handling. Do not eat, drink or smoke when using this product. IF SWALLOWED: Rinse mouth. Dispose of contents/container in accordance with local/regional/national/international regulations.