156965
Cyclohexanecarbonyl chloride
98%
Synonym(s):
Hexahydrobenzoyl chloride
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About This Item
Linear Formula:
C6H11COCl
CAS Number:
Molecular Weight:
146.61
Beilstein:
742163
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
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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Electrochemical reduction of cyclohexanecarbonyl chloride at mercury cathodes in acetonitrile.
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Journal of the Electrochemical Society, 140(4), 932-935 (1993)
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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
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