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About This Item
Linear Formula:
CH3(CH2)4C6H10CO2H
CAS Number:
Molecular Weight:
198.30
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
97%
form
solid
mp
51-53 °C (lit.)
functional group
carboxylic acid
SMILES string
CCCCC[C@@H]1CC[C@H](CC1)C(O)=O
InChI
1S/C12H22O2/c1-2-3-4-5-10-6-8-11(9-7-10)12(13)14/h10-11H,2-9H2,1H3,(H,13,14)/t10-,11-
InChI key
RVLAXPQGTRTHEV-XYPYZODXSA-N
Application
trans-4-Pentylcyclohexanecarboxylic acid has been used in preparation of:
- 4-[(2-(trans-4-pentylcyclohexyl)ethyl]phenol
- 4-[(4-trans-pentyl-cyclohexanecarbonyl)-(4-pyridin-4-yl-benzyl)-amino]-piperidine-1-tert-butyl carbamate
- 2-cyano-1-benzofuran-5-yl trans-4-pentylcyclohexanecarboxylate
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
235.4 °F - closed cup
Flash Point(C)
113 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Comparative studies of three-and four-ring mesogenic esters containing p-carborane, bicyclo [2.2. 2] octane, cyclohexane, and benzene
Ringstrand B, et al.
Liq. Cryst., 32(8), 1061-1070 (2005)
The synthesis and transition temperatures of 2-(4-alkyl-and 4-alkoxy-phenyl)-5-cyano-1-benzofurans and related diaryl-1-benzofurans-an assessment of how deviations from linearity and conformational effects in a core unit affect mesogenicity.
Friedman MR, et al.
Journal of Materials Chemistry, 11(11), 2759-2772 (2001)
Synthesis of plasmepsin II inhibitors-potential antimalarial agents
Mueller R, et al.
Molecules (Basel), 8(7), 556-564 (2003)
Beili Wang et al.
Environmental science & technology, 53(2), 1022-1030 (2018-12-18)
The nontargeted scanning chemical profiling approach has shown great potential to identify unknown pollutants or novel biological markers; however, the structure identification of unknown compounds is a challenge. In this study, a carboxyl-specific derivatization reagent, N-(4-aminomethylphenyl) pyridinium (AMPP), was coupled
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