CAS 6557-86-4
:Cycloheptanecarbonyl chloride
Description:
Cycloheptanecarbonyl chloride, with the CAS number 6557-86-4, is an organic compound characterized by a cycloheptane ring substituted with a carbonyl chloride functional group. This compound typically appears as a colorless to pale yellow liquid and has a distinctive odor. It is classified as an acyl chloride, which makes it reactive, particularly with nucleophiles, due to the presence of the carbonyl group adjacent to the chlorine atom. Cycloheptanecarbonyl chloride is soluble in organic solvents such as dichloromethane and ether but is generally insoluble in water. It is used in organic synthesis, particularly in the preparation of various chemical intermediates and in the development of pharmaceuticals. Due to its reactivity, it should be handled with care, as it can cause irritation to the skin, eyes, and respiratory system. Proper safety precautions, including the use of personal protective equipment, are essential when working with this compound.
Formula:C8H13ClO
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Found 4 products.
Cycloheptanecarbonyl chloride
CAS:Formula:C8H13ClOPurity:95%Color and Shape:LiquidMolecular weight:160.6412Cycloheptanecarbonyl chloride
CAS:Cycloheptanecarbonyl chloridePurity:95%Molecular weight:160.64g/molCycloheptanecarbonyl chloride
CAS:<p>Cycloheptanecarbonyl chloride (CHCl) is a chemical compound that has been shown to inhibit the growth of cancer cells. It is a pyrimidine compound with a basic structure and an active agent that inhibits the CB2 receptor. CHCl also reacts with nitro groups in benzimidazole compounds, which may lead to proliferation inhibitors. The heterocycle structures in CHCl are biologically active agents, especially for the treatment of leukemia. The high resistance of this compound makes it suitable for use in cancer treatments. Cycloheptanecarbonyl chloride can be synthesized by reacting sodium carbonate with cycloheptanone and hydrochloric acid.</p>Formula:C8H13ClOPurity:Min. 95%Molecular weight:160.64 g/mol




