TCI C0728 1,2-Cyclohexanedione (CAS 765-87-7) is a vicinal cyclic diketone widely used as a synthetic building block. Its adjacent carbonyl groups react readily with nitrogen nucleophiles, opening routes to fused heterocycles and chelating dioxime ligands. In protein chemistry it is a well-established reagent for the selective modification of arginine residues, supporting structure–function studies of enzymes and binding interfaces. AMI Scientific stocks 5 g and 25 g pack sizes; weigh the solid with appropriate protective equipment and store it tightly closed in a cool, dry, dark place.
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- Katrusiak (1993). Evidence for order-disorder phase transition coupled with large-amplitude intramolecular vibrations in 2-methyl-1,3-cyclohexanedione cyrstals. Solid State Communications doi:10.1016/0038-1098(93)90927-f
- Shen et al. (2011). The molecular structures and conformational compositions of 1,3 cyclohexanedione and 1,4 cyclohexanedione as determined by gas-phase electron diffraction and theoretical calculation. Journal of Molecular Structure doi:10.1016/j.molstruc.2011.08.043
- (1996). Cyclohexanedione oxygen scavengers. Applied Thermal Engineering doi:10.1016/1359-4311(96)82509-9
References were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.
