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Key Documents

101842

Sigma-Aldrich

Cyclohexanemethylamine

98%

Synonym(s):

(Aminomethyl)cyclohexane, Hexahydrobenzylamine

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About This Item

Linear Formula:
C6H11CH2NH2
CAS Number:
Molecular Weight:
113.20
Beilstein:
635751
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

98%

refractive index

n20/D 1.462 (lit.)

bp

159-161 °C (lit.)

density

0.87 g/mL at 25 °C (lit.)

functional group

amine

SMILES string

NCC1CCCCC1

InChI

1S/C7H15N/c8-6-7-4-2-1-3-5-7/h7H,1-6,8H2

InChI key

AVKNGPAMCBSNSO-UHFFFAOYSA-N

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Application

Cyclohexanemethylamine was used in the synthesis of Schiff′s base ligand, 4-methyl-2,6-bis(cyclohexylmethyliminomethyl)-phenol, which forms hexanuclear zinc(II) complexes. Cyclohexanemethylamine was used during the synthesis of 1-acyl-4 cycloalkyl/arylsemicarbazides and 1-acyl-5-benzyloxy/hydroxyl carbamoylcarbazides from the nonsteroidal anti-inflammatory drugs.

Pictograms

FlameCorrosion

Signal Word

Danger

Hazard Statements

Hazard Classifications

Flam. Liq. 3 - Skin Corr. 1B

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

118.4 °F - closed cup

Flash Point(C)

48 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Synthesis, characterization and fluorescence properties of hexanuclear zinc (II) complexes.
Roy P, et al.
Polyhedron, 28(6), 1133-1137 (2009)
I Perković et al.
European journal of medicinal chemistry, 51, 227-238 (2012-03-13)
The novel 1-acyl-4-cycloalkyl/arylsemicarbazides (5a-y) and 1-acyl-5-benzyloxy/hydroxycarbamoylcarbazides (8a-f) derived from the nonsteroidal anti-inflammatory drugs ibuprofen, fenoprofen and reduced ketoprofen were prepared, fully chemically characterized and evaluated for their cytostatic, antiviral and antioxidant activities. Compounds 5 and 8 consist of a region

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