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261602

Sigma-Aldrich

trans-4-Pentylcyclohexanecarboxylic acid

97%

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About This Item

Linear Formula:
CH3(CH2)4C6H10CO2H
CAS Number:
38289-29-1
Molecular Weight:
198.30
MDL number:
MFCD00009964
UNSPSC Code:
12352100
PubChem Substance ID:
24855823
NACRES:
NA.22

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

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319

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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Certificates of Analysis (COA)

Lot/Batch Number
MKCS9877
MKCT4253
MKCC5606
MKBT4839V
MKBQ2187V

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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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