5-Chlorocyclopenta-1,3-diene, also known as chlorocyclopentane, is an organic compound characterized by its cyclic structure featuring a five-membered carbon ring with two double bonds and a chlorine substituent. The presence of the chlorine atom introduces unique reactivity, making it a potential candidate for various chemical reactions, including electrophilic substitutions and nucleophilic additions. This compound is typically a colorless to pale yellow liquid with a distinctive odor. Its reactivity is influenced by the conjugated diene system, which can participate in Diels-Alder reactions or polymerization processes. The compound's physical properties, such as boiling point and solubility, are affected by the chlorine substituent and the cyclic structure. As for its safety and handling, it is essential to consider its potential toxicity and environmental impact, necessitating appropriate precautions during use. The CAS number 1293-67-0 uniquely identifies this compound in chemical databases, facilitating its study and application in various fields, including organic synthesis and materials science.

5-chlorocyclopenta-1,3-diene; chlorocyclopentane; iron

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1,1'-Dichloroferrocene is a molecule that belongs to the group of benzenes and has a gaseous form. It has potential energy and is an optical active compound. 1,1'-Dichloroferrin can be found in synchrotron radiation and it's optical absorption is dipole. The ligand for 1,1'-dichloroferrocene is ferrocene. This molecule transfers energy through radiation and optical excitation. The parameters for bromoferrocene are similar to those of 1,1'-dichloroferrin except that it does not have the same steric properties.

CAS 1293-67-0: 5-chlorocyclopenta-1,3-diene; chlorocyclopentane; iron

1,1'-Dichloroferrocene

Ref: 3D-FD163271