Cyclohexanecarbonyl chloride, 97+%
Cyclohexanecarbonyl chloride, 97+%
Cyclohexanecarbonyl chloride, 97+%
Thermo Scientific Chemicals

Cyclohexanecarbonyl chloride, 97+%

CAS: 2719-27-9 | C7H11ClO | 146.61 g/mol
Quantity:
25 g
100 g
Catalog number A19824.14
also known as A19824-14
Price (JPY)
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Quantity:
25 g
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Chemical Identifiers
CAS2719-27-9
IUPAC Namecyclohexanecarbonyl chloride
Molecular FormulaC7H11ClO
InChI KeyRVOJTCZRIKWHDX-UHFFFAOYSA-N
SMILESClC(=O)C1CCCCC1
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SpecificationsSpecification SheetSpecification Sheet
FormLiquid
Assay (GC)≥97.0%
Refractive Index1.4670-1.4720 @ 20°C (non-U.S. specification)
Appearance (Color)Clear colorless to pale yellow
Cyclohexanecarbonyl chloride is 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.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Cyclohexanecarbonyl chloride is 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.

Solubility
Reacts with water.

Notes
Moisture Sensitive. Store away from strong oxidizing agents. Keep container tightly closed. Store in cool, dry conditions in well sealed containers.
RUO – Research Use Only

General References:

  1. Scott C. Berk.; Paul Knochel.; Ming Chang P. Yeh. General approach to highly functionalized benzylic organometallics of zinc and copper. J. Org. Chem. 1988, 53, (24), 5789-5791
  2. A. C. Poshkus.; J. E. Herweh. A New Reaction between Cyclohexanecarbonyl Chloride and Phenyl Isocyanate. J. Org. Chem. 1965, 30, (7), 2466-2469