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β-Dihydro-heptachlor, also known as heptachlor epoxide, is a chemical compound derived from heptachlor, an organochlorine pesticide. It is formed as a result of the reduction of heptachlor, and it is more toxic and persistent in the environment than its parent compound. β-Dihydro-heptachlor is a white crystalline solid with a chemical formula of C10H5Cl7O. It is known for its high stability, resistance to degradation, and bioaccumulation in the food chain, which has led to its classification as a persistent organic pollutant (POP). Due to its potential health risks and environmental impact, the use of heptachlor and its derivatives, including β-Dihydro-heptachlor, has been banned or restricted in many countries.

5039-62-3

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5039-62-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5039-62-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,3 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5039-62:
(6*5)+(5*0)+(4*3)+(3*9)+(2*6)+(1*2)=83
83 % 10 = 3
So 5039-62-3 is a valid CAS Registry Number.

5039-62-3Upstream product

5039-62-3Downstream Products

5039-62-3Relevant academic research and scientific papers

Role of water traces in the liquid-phase catalytic hydrochlorination of olefins in organic solvents

Mal'kov,Romm,Abronin

, p. 243 - 246 (1998)

The liquid-phase hydrochlorination of 4,5,6,7,8,8,-hexachloro-3′,4,7,7′-tetrahydro-4,7-methanoindene (Chlordene) catalyzed by gallium or aluminum halides occurs in the presence of water traces in an aprotic organic solvent. Complexes H2O · M2X6, where M is metal and X is halogen, catalyze this reaction. The reaction proceeds under homogeneous conditions. Under heterogeneous catalytic conditions, the solid phase in the AlCl3-CCl4 system attains the required concentration of AlCl3 in the solution. It was shown using quantum-chemical PM3 calculations that the water molecule facilitates the transfer of proton in the form of the hydroxonium ion from an HCl molecule to olefin.

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