161470
3-Cyclohexanepropionic acid
99%
Synonym(s):
3-Cyclohexylpropionic acid
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50 G
$402.00
About This Item
Linear Formula:
C6H11CH2CH2CO2H
CAS Number:
Molecular Weight:
156.22
Beilstein/REAXYS Number:
2042799
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
form:
liquid
assay:
99%
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Quality Level
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.[1]
- To synthesize chemical intermediates such as cyclohexanepropanenitrile [2], cyclohexanepropanamide [3], cyclohexanepropanol [4], and 1-oxaspiro[4.5]decan-2-one [5].
Biochem/physiol Actions
3-Cyclohexanepropionic acid facilitates oral delivery of cromolyn via permeation across/through the membrane in rats[6].
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2
Storage Class
10 - Combustible liquids
wgk_germany
WGK 3
flash_point_f
266.0 °F
flash_point_c
130 °C
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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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)
Remote Allylation of Unactivated C (sp3)-H Bonds Triggered by Photogenerated Amidyl Radicals
Xu B and Tambar UK
ACS Catalysis, 21(7), 947-955 (2019)
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)
C-H oxygenation at tertiary carbon centers using iodine oxidant
Kiyokawa K, et al.
Chemical Communications (Cambridge, England), 54(55), 7609-7612 (2018)
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