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Merck
CN

28972

Cyclohexanecarboxaldehyde

technical, ≥90% (GC)

Synonym(s):

Hexahydrobenzaldehyde

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About This Item

Linear Formula:
C6H11CHO
CAS Number:
2043-61-0
Molecular Weight:
112.17
EC Number:
218-057-7
UNSPSC Code:
12352100
PubChem Substance ID:
329753300
Beilstein/REAXYS Number:
878306
MDL number:
MFCD00001457
Assay:
≥90% (GC)

Key Documents

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InChI key

KVFDZFBHBWTVID-UHFFFAOYSA-N

InChI

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

SMILES string

O=CC1CCCCC1

grade

technical

assay

≥90% (GC)

Quality Level

100

bp

161-163 °C (lit.)

density

0.926 g/mL at 25 °C (lit.)

storage temp.

2-8°C

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Disclaimer

may become turbid on storage

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

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

Regulatory Information

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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)
[Mn(tmc)(O2)]+: a side-on peroxido manganese(III) complex bearing a non-heme ligand.
Mi Sook Seo et al.
Angewandte Chemie (International ed. in English), 46(3), 377-380 (2006-11-30)
Ashfaq Ahmad et al.
Drug design, development and therapy, 14, 2165-2178 (2020-07-02)
The current study was designed to synthesize derivatives of succinimide and compare their biological potency in anticholinesterase, alpha-glucosidase inhibition, and antioxidant assays. In this research, two succinimide derivatives including (S)-1-(2,5-dioxo-1-phenylpyrrolidin-3-yl) cyclohexanecarbaldehyde (Compound 1) and (R)-2-((S)-2,5-dioxo-1-phenylpyrrolidin-3-yl)-2-phenylpropanal (Compound 2) were synthesized using

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