156965
Cyclohexanecarbonyl chloride
98%
Synonym(s):
Hexahydrobenzoyl chloride
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About This Item
Linear Formula:
C6H11COCl
CAS Number:
Molecular Weight:
146.61
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
220-322-7
Beilstein/REAXYS Number:
742163
MDL number:
Assay:
98%
Form:
liquid
assay
98%
form
liquid
InChI key
RVOJTCZRIKWHDX-UHFFFAOYSA-N
InChI
1S/C7H11ClO/c8-7(9)6-4-2-1-3-5-6/h6H,1-5H2
SMILES string
ClC(=O)C1CCCCC1
Quality Level
bp
184 °C (lit.)
density
1.096 g/mL at 25 °C (lit.)
functional group
acyl chloride
Related Categories
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
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B - STOT SE 3
target_organs
Respiratory system
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 1
flash_point_f
150.8 °F
flash_point_c
66 °C
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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Hakan Arslan et al.
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.
Urove GA and Peters DG.
Journal of the Electrochemical Society, 140(4), 932-935 (1993)
Shigeo Hayashi et al.
Journal of enzyme inhibition and medicinal chemistry, 29(6), 846-867 (2014-02-13)
Because of the pivotal role of cyclooxygenase (COX) in the inflammatory processes, non-steroidal anti-inflammatory drugs (NSAIDs) that suppress COX activities have been used clinically for the treatment of inflammatory diseases/syndromes; however, traditional NSAIDs exhibit serious side-effects such as gastrointestinal damage
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