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108464

Sigma-Aldrich

Cyclohexanecarboxaldehyde

97%

Synonym(s):

Hexahydrobenzaldehyde

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About This Item

Linear Formula:
C6H11CHO
CAS Number:
2043-61-0
Molecular Weight:
112.17
Beilstein/REAXYS Number:
878306
EC Number:
218-057-7
MDL number:
MFCD00001457
UNSPSC Code:
12352100
PubChem Substance ID:
24846806
NACRES:
NA.22

Quality Level

100

assay

97%

refractive index

n20/D 1.452 (lit.)

bp

161-163 °C (lit.)

density

0.926 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

O=CC1CCCCC1

InChI

1S/C7H12O/c8-6-7-4-2-1-3-5-7/h6-7H,1-5H2

InChI key

KVFDZFBHBWTVID-UHFFFAOYSA-N

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Application

Cyclohexanecarboxaldehyde was used to study gas-phase microwave spectrum of cyclohexanecarboxaldehyde. It was used for the synthesis of poly(vinyl cyclohexanal). It was used as model substrate in the synthesis of propargylamines using Fe3O4 nanoparticles as catalyst. It was employed in an aldol reaction with ethyl diazoacetate catalyzed by basic, nanoparticulate magnesium oxide leading to α-diazo-β-hydroxyesters.

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

105.8 °F - closed cup

flash_point_c

41 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Acid formation in polymer solids by radiation-induced chain reactions of diphenyliodonium salts.
Koizumi H, et al.
Radiation Physics and Chemistry, 80(2), 190-195 (2011)
Tetrahedron Letters, 48, 6121-6121 (2007)
Conformational study of cyclohexanecarboxaldehyde by microwave spectroscopy.
Kao PN and Turner PH.
Journal of the American Chemical Society, 101(16), 4497-4499 (1979)
Magnetically separable Fe3 O4 nanoparticles: an efficient catalyst for the synthesis of propargylamines.
Sreedhar B, et al.
Tetrahedron Letters, 51(14), 1891-1895 (2010)
Differential inactivation of DNA polymerases alpha and beta by aldehyde compounds.
K Suzuki et al.
Biochemical and biophysical research communications, 100(4), 1626-1633 (1981-06-01)
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