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Sigma-Aldrich

3-Cyclohexanepropionic acid

99%

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Synonym(s):
3-Cyclohexylpropionic acid
Linear Formula:
C6H11CH2CH2CO2H
CAS Number:
701-97-3
Molecular Weight:
156.22
Beilstein:
2042799
EC Number:
211-861-9
MDL number:
MFCD00001527
UNSPSC Code:
12352100
PubChem Substance ID:
24849930
NACRES:
NA.22

Quality Level

100

Assay

99%

form

liquid

refractive index

n20/D 1.464 (lit.)

bp

275.8 °C (lit.)

mp

14-17 °C (lit.)

density

0.912 g/mL at 25 °C (lit.)

SMILES string

OC(=O)CCC1CCCCC1

InChI

1S/C9H16O2/c10-9(11)7-6-8-4-2-1-3-5-8/h8H,1-7H2,(H,10,11)

InChI key

HJZLEGIHUQOJBA-UHFFFAOYSA-N

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Application

3-Cyclohexanepropionic acid can be used:
  • As a starting material in the synthesis of 2-[(1,2,4-triazol-3-yl)thio]acetamide derivatives for in vitro paraoxonase-1 (PON1) studies.
  • To synthesize chemical intermediates such as cyclohexanepropanenitrile , cyclohexanepropanamide , cyclohexanepropanol , and 1-oxaspiro[4.5]decan-2-one .

Biochem/physiol Actions

3-Cyclohexanepropionic acid facilitates oral delivery of cromolyn via permeation across/through the membrane in rats.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302,H315,H319

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2

WGK

WGK 3

Flash Point(F)

266.0 °F

Flash Point(C)

130 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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A Leone-Bay et al.
Pharmaceutical research, 13(2), 222-226 (1996-02-01)
Herein we report the discovery of a group of derivatized alpha-amino acids that increase the oral bioavailability of sodium cromolyn. We prepared three N-acylated alpha-amino acids and used these compounds to demonstrate the oral delivery of cromolyn in an in
Synthesis and evaluation of novel 2-[(1, 2, 4-triazol-3-yl) thio] acetamide derivatives as potential serum paraoxonase-1 (PON1) activators
YURTTA L, et al.
Marmara Pharmaceutical Journal, 21(4), 967-977 (2017)
Ethylenation of aldehydes to 3-propanal, propanol and propanoic acid derivatives
Payne DT, et al.
Scientific reports, 7(1), 1720-1720 (2017)
C-H oxygenation at tertiary carbon centers using iodine oxidant
Kiyokawa K, et al.
Chemical Communications (Cambridge, England), 54(55), 7609-7612 (2018)
Continuous flow synthesis under high-temperature/high-pressure conditions using a resistively heated flow reactor
Adeyemi A, et al.
Organic Process Research & Development, 21(7), 947-955 (2017)
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