6629-96-5 Usage
Chemical structure
A 1,4-dioxane ring with seven chlorine atoms attached.
Chemical stability
High degree of chemical stability, making it difficult to break down and eliminate from the environment.
Environmental persistence
Due to its persistent nature, it poses a potential risk to human health and the environment.
Carcinogenic potential
Considered a potential carcinogen.
Accumulation in soil and water
Found to accumulate in soil and water, posing a threat to aquatic ecosystems.
Industrial use
Limited industrial use.
Byproduct in chemical processes
May be an unintended byproduct of certain chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 6629-96-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,2 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6629-96:
(6*6)+(5*6)+(4*2)+(3*9)+(2*9)+(1*6)=125
125 % 10 = 5
So 6629-96-5 is a valid CAS Registry Number.
6629-96-5Relevant academic research and scientific papers
Perhalodioxins and Perhalodihydrodioxins
Krespan, Carl G.,Dixon, David A.
, p. 3915 - 3923 (2007/10/02)
Two perhalo-1,4-dihydrodioxins, representatives of a previously unknown class of compounds, have been synthesized and shown to exhibit unusual reactivity.In particular, reaction with oxygen is spontaneous and exothermic, and radical-catalyzed homopolymerization will proceed through a fluorinated double bond.Representatives of the perhalo-2,3-dihydro-1,4-dioxin class have also been prepared and found to have reactivity in general intermediate to that of the perhalodioxoles and acyclic trifluorovinyl ethers.Computational studies of the two systems established thatintroduction of the first double bond raises the energy substantially, while the second double bond results in a near-planar ring with dramatically increased energy content.
