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Merck
CN

161470

3-Cyclohexanepropionic acid

99%

Synonym(s):

3-Cyclohexylpropionic acid

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About This Item

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

Key Documents

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Product Name

3-Cyclohexanepropionic acid, 99%

InChI key

HJZLEGIHUQOJBA-UHFFFAOYSA-N

InChI

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

SMILES string

OC(=O)CCC1CCCCC1

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.)

Quality Level

100

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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

signalword

Warning

Hazard Classifications

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

Storage Class

10 - Combustible liquids

wgk

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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Certificates of Analysis (COA)

Lot/Batch Number
SHBJ6756
SHBH8808
SHBF9890V
SHBF9889V
SHBF1725V

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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)
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)
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