101842
Cyclohexanemethylamine
98%
Synonym(s):
(Aminomethyl)cyclohexane, Hexahydrobenzylamine
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About This Item
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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.
Signal Word
Danger
Hazard Statements
Precautionary 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.
Polyhedron, 28(6), 1133-1137 (2009)
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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