Search results
Results from the WOW.Com Content Network
2,2,4,4-Tetramethylcyclobutane-1,3-dione. Other names ... (CH 3) 4 C 4 O 2. The compound is a diketone of cyclobutane, bearing four methyl groups. It is a white solid ...
2,2,4,4-Tetramethyl-1,3-cyclobutanediol (CBDO) is an aliphatic diol. This diol is produced as a mixture of cis- and trans-isomers, depending on the relative stereochemistry of the hydroxyl groups. It is used as a monomer for the synthesis of polymeric materials, usually as an alternative to bisphenol A (BPA).
Tetramethylbutane, sometimes called hexamethylethane, is a hydrocarbon with formula C 8 H 18 or (H 3 C-) 3 C-C(-CH 3) 3. It is the most heavily branched and most compact of the octane isomers, the only one with a butane (C4) backbone. Because of its highly symmetrical structure, it has a very high melting point and a short liquid range; in fact ...
The unsubstituted [4]radialene has been prepared in an elimination reaction of cis,trans,cis-tetra(bromomethyl)cyclobutane with sodium methoxide in ethanol. [25] [4]radialene synthesis. Hydrogenation with platinum on carbon gives cis,cis,cis-tetramethylcyclobutane in accordance with the proposed structure.
It can be prepared by base-catalyzed isomerization of 2,3-dimethyl-1-butene. [2] Another route involves direct dimerization of propylene. [3] It can also be produced by photolysis of tetramethylcyclobutane-1,3-dione. [4]
Cyclohexane-1,2,3,4,5,6-hexol is a family of chemical compounds with formula C 6 H 12 O 6, whose molecule consists of a ring of six carbon atoms, each bound to one hydrogen atom and one hydroxyl group (–OH).
Get AOL Mail for FREE! Manage your email like never before with travel, photo & document views. Personalize your inbox with themes & tabs. You've Got Mail!
1,2,3,4-Butanetetracarboxylic acid is an organic compound with the formula HO 2 CCH 2 CH(CO 2 H)CH(CO 2 H)CH 2 CO 2 H. It is one of the simplest stable tetracarboxylic acids. The compound exists as two diastereomers, meso and the (R,R)/(S,S) pair. All are white solids. The compound is produced by oxidation of tetrahydrophthalic anhydride. [1]