B92001
4-tert-Butylcyclohexanol, mixture of cis and trans
98%
Sign Into View Organizational & Contract Pricing
All Photos(2)
About This Item
Recommended Products
Assay
98%
form
powder
bp
110-115 °C/15 mmHg (lit.)
mp
62-70 °C (lit.)
SMILES string
CC(C)(C)C1CCC(O)CC1
InChI
1S/C10H20O/c1-10(2,3)8-4-6-9(11)7-5-8/h8-9,11H,4-7H2,1-3H3
InChI key
CCOQPGVQAWPUPE-UHFFFAOYSA-N
Application
4-tert-Butylcyclohexanol (mixture of cis and trans) can be used as a reactant to synthesize tris(4,4′-di-tert-butyl-2,2′-bipyridine)(trans-4-tert-butylcyclohexanolato)deca-μ-oxido-heptaoxidoheptavanadium oxide cluster complex by reacting with [V8O20(C18H24N2)4]. It can also be used as a reactant in competitive Oppenauer oxidation experiments in the presence of zeolite BEA as a stereoselective catalyst. Only cis-isomer is selectively converted to the corresponding ketone, whereas trans-isomer remains unchanged.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 1
Flash Point(F)
221.0 °F - closed cup
Flash Point(C)
105 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Certificates of Analysis (COA)
Don't see the Right Version?
If you require a particular version, you can look up a specific certificate by the Lot or Batch number.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Stereoselective Meerwein-Ponndorf-Verley and Oppenauer reactions catalysed by zeolite BEA
J. Mol. Catal. A: Chem., 115(3), 457-472 (1997)
Tris (4, 4?-di-tert-butyl-2, 2?-bipyridine)(trans-4-tert-butylcyclohexanolato) deca- ? -oxido-heptaoxidoheptavanadium acetonitrile monosolvate including another unknown solvent molecule
IUCrData, 5(4), x200449-x200449 (2020)
Journal of analytical methods in chemistry, 2012, 452949-452949 (2012-06-01)
The use of iodine as a catalyst and either acetic or trifluoroacetic acid as a derivatizing reagent for determining the enantiomeric composition of acyclic and cyclic aliphatic chiral alcohols was investigated. Optimal conditions were selected according to the molar ratio
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service