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374938

Sigma-Aldrich

4-tert-Butylcyclohexanecarboxylic acid

99%

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About This Item

Linear Formula:
(CH3)3CC6H10CO2H
CAS Number:
Molecular Weight:
184.28
Beilstein:
2043187
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
EC Index Number:
611-163-8
NACRES:
NA.22

Assay

99%

form

solid

mp

148 °C (lit.)

SMILES string

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)

InChI key

QVQKEGYITJBHRQ-UHFFFAOYSA-N

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General description

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.

Application

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.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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C L Perrin et al.
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
Conformational analysis. LXXV. Methylation rates of cis-and trans-4-tert-butyl-N, N-dimethylcyclohexylamines.
Allinger NL and Graham JC.
The Journal of Organic Chemistry, 36(12), 1688-1690 (1971)
Yanqing Liu et al.
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

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