B92001
4-叔丁基环己醇，顺式和反式混合物
98%
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关于此项目
线性分子式:
(CH3)3CC6H10OH
化学文摘社编号:
分子量:
156.27
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-676-4
Beilstein/REAXYS Number:
1902277
MDL number:
产品名称
4-叔丁基环己醇，顺式和反式混合物, 98%
InChI key
CCOQPGVQAWPUPE-UHFFFAOYSA-N
InChI
1S/C10H20O/c1-10(2,3)8-4-6-9(11)7-5-8/h8-9,11H,4-7H2,1-3H3
SMILES string
CC(C)(C)C1CCC(O)CC1
assay
98%
form
powder
bp
110-115 °C/15 mmHg (lit.)
mp
62-70 °C (lit.)
Application
4-叔-正丁基环己醇（顺式和反式混合物）可作为反应物，用于合成三（4,4′-二-叔-丁基-2,2′- 联吡啶）（反式-4-叔-丁基环己醇）十-μ-氧化-七氧化七氧化钒簇合物，通过与[V8O20(C18H24N2)4]反应。还可以沸石BEA作为立体选择性催化剂，用作竞争对手Oppenauer氧化实验的反应物。仅将顺式-异构体选择性转化为对应的酮，而顺式-异构体保持不变。
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2
存储类别
11 - Combustible Solids
wgk
WGK 1
flash_point_f
221.0 °F - closed cup
flash_point_c
105 °C - closed cup
ppe
Eyeshields, Gloves, type N95 (US)
Tris (4, 4?-di-tert-butyl-2, 2?-bipyridine)(trans-4-tert-butylcyclohexanolato) deca- ? -oxido-heptaoxidoheptavanadium acetonitrile monosolvate including another unknown solvent molecule
Kodama S, et al.
IUCrData, 5(4), x200449-x200449 (2020)
Stereoselective Meerwein-Ponndorf-Verley and Oppenauer reactions catalysed by zeolite BEA
Creyghton EJ, et al.
J. Mol. Catal. A: Chem., 115(3), 457-472 (1997)
Mireia Oromí-Farrús et al.
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
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