156965
Cyclohexanecarbonyl chloride
98%
Synonym(s):
Hexahydrobenzoyl chloride
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Assay
98%
form
liquid
refractive index
n20/D 1.469 (lit.)
bp
184 °C (lit.)
density
1.096 g/mL at 25 °C (lit.)
functional group
acyl chloride
SMILES string
ClC(=O)C1CCCCC1
InChI
1S/C7H11ClO/c8-7(9)6-4-2-1-3-5-6/h6H,1-5H2
InChI key
RVOJTCZRIKWHDX-UHFFFAOYSA-N
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General description
Electrochemical reduction of cyclohexanecarbonyl chloride at a hanging mercury drop electrode in acetonitrile has been reported.
Application
Cyclohexanecarbonyl chloride was used in the preparation of five thiourea derivative ligands having anti-bacterial and anti-yeast activity:
- (N-(diethylcarbamothioyl)cyclohexanecarboxamide
- N-(di-n-propylcarbamothioyl)cyclohexanecarboxamide
- di-n-butylcarbamothioyl)cyclohexanecarboxamide
- N-(diphenylcarbamothioyl)cyclohexanecarboxamide
- N-(morpholine-4-carbonothioyl)cyclohexanecarboxamide
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 1
Flash Point(F)
150.8 °F
Flash Point(C)
66 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Molecules (Basel, Switzerland), 14(1), 519-527 (2009-01-27)
Five thiourea derivative ligands and their Ni(2+) and Cu(2+) complexes have been synthesized. The compounds were screened for their in vitro anti-bacterial activity using Gram-positive bacteria (two different standard strains of Staphylococcus aureus, Staphylococcus epidermidis, Enterococcus faecalis, Streptococcus pyogenes, Bacillus
Electrochemical reduction of cyclohexanecarbonyl chloride at mercury cathodes in acetonitrile.
Journal of the Electrochemical Society, 140(4), 932-935 (1993)
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