374938
4-tert-Butylcyclohexanecarboxylic acid
99%
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About This Item
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Nível de qualidade
Ensaio
99%
forma
solid
pf
148 °C (lit.)
grupo funcional
carboxylic acid
cadeia de caracteres SMILES
CC(C)(C)C1CCC(CC1)C(O)=O
InChI
1S/C11H20O2/c1-11(2,3)9-6-4-8(5-7-9)10(12)13/h8-9H,4-7H2,1-3H3,(H,12,13)
chave InChI
QVQKEGYITJBHRQ-UHFFFAOYSA-N
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Descrição geral
delta pKa between the two stereoisomers of 4-tert-butylcyclohexanecarboxylic acid has been studied using 1H and 13C NMR. Preparation of cis- and trans-4-tert- butylcyclohexanecarboxylic acid has been reported.
Aplicação
4-tert-Butylcyclohexanecarboxylic acid may be used in the preparation of N-((S)-3-(4-(7-chloroquinolin-4-yl)piperazin-1-yl)-1-henylpropyl)-4-tert-butylcyclohexanecarboxamide.
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
Eyeshields, Gloves, type N95 (US)
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Conformational analysis. LXXV. Methylation rates of cis-and trans-4-tert-butyl-N, N-dimethylcyclohexylamines.
The Journal of Organic Chemistry, 36(12), 1688-1690 (1971)
Molecules (Basel, Switzerland), 13(10), 2426-2441 (2008-10-03)
CCR5, as the major co-receptor for HIV-1 entry, is an attractive novel target for the pharmaceutical industry in the HIV-1 therapeutic area. In this study, based on the structures of maraviroc and 1,4-bis(4-(7-chloroquinolin-4-yl)piperazin-1-yl)butane-1,4-dione (1), which was identified using structure-based virtual
Analytical chemistry, 68(13), 2127-2134 (1996-07-01)
An NMR titration method has been developed to simultaneously measure the difference in acid dissociation constants (delta pKa) of two or more compounds with high precision and accuracy. The delta pKa between the conjugate acids of the two stereoisomers of
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