CAS 2719-27-9
:Cyclohexanecarbonyl chloride
Description:
Cyclohexanecarbonyl chloride, with the CAS number 2719-27-9, is an organic compound characterized by its carbonyl chloride functional group attached to a cyclohexane ring. It is a colorless to pale yellow liquid that is typically used as an acylating agent in organic synthesis. The presence of the carbonyl chloride group makes it reactive, particularly towards nucleophiles, allowing it to participate in various chemical reactions, such as acylation of amines and alcohols. Cyclohexanecarbonyl chloride has a relatively low boiling point and is soluble in organic solvents, but it is not soluble in water due to its hydrophobic cyclohexane structure. Safety precautions are necessary when handling this compound, as it can be corrosive and may release toxic gases upon hydrolysis. Its applications extend to the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals, making it a valuable intermediate in chemical manufacturing. Proper storage in a cool, dry place away from moisture is essential to maintain its stability and reactivity.
Formula:C7H11ClO
InChI:InChI=1S/C7H11ClO/c8-7(9)6-4-2-1-3-5-6/h6H,1-5H2
InChI key:InChIKey=RVOJTCZRIKWHDX-UHFFFAOYSA-N
SMILES:C(Cl)(=O)C1CCCCC1
Synonyms:- (Chlorocarbonyl)cyclohexane
- 7-Ethyl-3-(2-hydroxyethyl)indole
- Chlorure de cyclohexanecarbonyle
- Cloruro De Ciclohexanocarbonilo
- Cyclohexancarbonylchlorid
- Cyclohexanecarbonyl chloride
- Cyclohexanoic acid chloride
- Cyclohexanoyl chloride
- Cyclohexyl Carboxylic Acid Chloride
- Cyclohexylcarbonyl chloride
- Cyclotexaformyl Chloride
- Hexahydrobenzoyl chloride
- Nsc 85181
- See more synonyms
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Found 8 products.
Cyclohexanecarbonyl Chloride
CAS:Formula:C7H11ClOPurity:>98.0%(GC)Color and Shape:Colorless to Light yellow clear liquidMolecular weight:146.61Cyclohexanecarbonyl chloride, 97+%
CAS:<p>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-(diphenylc</p>Formula:C7H11ClOPurity:97+%Color and Shape:Liquid, Clear colorless to pale yellowMolecular weight:146.61Cyclohexanecarbonyl chloride
CAS:Formula:C7H11ClOPurity:96%Color and Shape:LiquidMolecular weight:146.6146Cyclohexanecarbonyl chloride
CAS:<p>Cyclohexanecarbonyl chloride</p>Purity:96%Molecular weight:146.62g/molCyclohexanecarbonyl Chloride
CAS:Controlled Product<p>Applications Cyclohexanecarbonyl Chloride is used to prepare 1,2,3-triazoles as inhibitors of human immunodeficiency virus type 1 protease. It was also used to synthesize benzothiazole as potent antitumor agents.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Whiting, M., et al.: J. Med. Chem., 49, 7697 (2006); Yoshida, M., et al.: Bioorg. Med. Chem. Lett., 15, 3328 (2005)<br></p>Formula:C7H11ClOColor and Shape:NeatMolecular weight:146.61Cyclohexanecarbonyl chloride
CAS:Formula:C7H11ClOPurity:95.0%Color and Shape:LiquidMolecular weight:146.61Cyclohexanecarbonyl-d11 Chloride
CAS:Controlled Product<p>Applications Cyclohexanecarbonyl-d11 Chloride is labelled Cyclohexanecarbonyl Chloride which is used to prepare 1,2,3-triazoles as inhibitors of human immunodeficiency virus type 1 protease. It was also used to synthesize benzothiazole as potent antitumor agents.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Whiting, M., et al.: J. Med. Chem., 49, 7697 (2006); Yoshida, M., et al.: Bioorg. Med. Chem. Lett., 15, 3328 (2005)<br></p>Formula:C7D11ClOColor and Shape:NeatMolecular weight:157.68Cyclohexanecarbonyl chloride
CAS:<p>Cyclohexanecarbonyl chloride is a chemical compound that is used in the treatment of wastewater. It is also used as an antidiabetic agent, and has been shown to have anti-inflammatory and immunosuppressive properties. Cyclohexanecarbonyl chloride is a reactive intermediate that can be prepared by acylation of benzimidazole compounds with cyclohexane rings containing a hydroxyl group. This reaction yields a 1:1 mixture of the two products, which are identical except for their configuration at the benzylic position.</p>Formula:C7H11ClOPurity:Min. 95%Color and Shape:Colourless To Yellow LiquidMolecular weight:146.61 g/mol






