CAS 163119-16-2: 2,6-Bis-tert-butyl-4-methylcyclohexanol
Formula:C15H30O
InChI:InChI=1S/C15H30O/c1-10-8-11(14(2,3)4)13(16)12(9-10)15(5,6)7/h10-13,16H,8-9H2,1-7H3
InChI key:InChIKey=OIXQKWDQCODZGF-UHFFFAOYSA-N
SMILES:C(C)(C)(C)C1C(O)C(C(C)(C)C)CC(C)C1
Synonyms:- 2,6-Bis(1,1-Dimethylethyl)-4-Methylcyclohexanol
- 2,6-Di-tert-butyl-4-methylcyclohexan-1-ol
- 2,6-Di-tert-butyl-4-methylcyclohexanol
- 2,6-Ditert-butyl-4-methylcyclohexan-1-ol
- Cyclohexanol, 2,6-bis(1,1-dimethylethyl)-4-methyl-
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Found 4 products.
2,6-Di(tert-butyl)-4-methylcyclohexan-1-ol
CAS:2,6-Di(tert-butyl)-4-methylcyclohexan-1-olFormula:C15H30OPurity:97%Color and Shape: colourless liquidMolecular weight:226.40g/mol2,6-Di-tert-butyl-4-methylcyclohexanol
CAS:Purity:95.0%Color and Shape:SolidMolecular weight:226.4040069580078Cyclohexanol, 2,6-bis(1,1-dimethylethyl)-4-methyl-
CAS:Formula:C15H30OPurity:95%Color and Shape:SolidMolecular weight:226.39812,6-Bis-tert-butyl-4-methylcyclohexanol
CAS:2,6-Bis-tert-butyl-4-methylcyclohexanol is a synthetic chemical that is used as an agrochemical. It can be produced by the hydrogenation of 2,6-bis(tert-butyl)-4-methylcyclohexene. This reaction requires a catalyst such as magnesium or nickel and hydrochloric acid to reduce the alkali metal chloride in the xylene to form 2,6-bis(tert-butyl)-4-methylcyclohexanol. The compound has been shown to have good selectivity for chlorides and other halides. It can also be synthesized from 2,6-dichlorocyclohexane with sodium methoxide in methanol solvent at low temperatures.Formula:C15H30OPurity:Min. 95%Molecular weight:226.4 g/mol
