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108464

Sigma-Aldrich

Cyclohexanecarboxaldehyde

97%

Synonym(s):

Hexahydrobenzaldehyde

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About This Item

Linear Formula:
C6H11CHO
CAS Number:
Molecular Weight:
112.17
Beilstein:
878306
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

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

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

105.8 °F - closed cup

Flash Point(C)

41 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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