15012-64-3 Usage
Uses
Given the highly toxic nature of 2,3,6,7-tetrachloro-5,8-dihydroxy-1,4-naphthoquinone (TCDD), it does not have typical applications like other chemicals in various industries. Instead, the focus is on its management and mitigation due to its hazardous properties. However, for the sake of understanding its relevance, the following points can be considered:
Used in Environmental Monitoring and Research:
TCDD is utilized as a subject of study in environmental monitoring and research to understand its distribution, impact, and methods for reduction in the environment. This helps in developing strategies for pollution control and prevention.
Used in Regulatory Frameworks:
TCDD serves as a reference point in regulatory frameworks aimed at controlling the emission of dioxins and related compounds in industrial processes. Its inclusion in these frameworks is crucial for setting safety standards and permissible limits.
Used in Public Health Initiatives:
In public health initiatives, TCDD is a focal point for raising awareness about the risks associated with exposure to dioxins and the importance of minimizing environmental contamination.
Check Digit Verification of cas no
The CAS Registry Mumber 15012-64-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,0,1 and 2 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 15012-64:
(7*1)+(6*5)+(5*0)+(4*1)+(3*2)+(2*6)+(1*4)=63
63 % 10 = 3
So 15012-64-3 is a valid CAS Registry Number.
15012-64-3Relevant academic research and scientific papers
Cycloacylation of chloro-substituted hydroquinone dimethyl ethers with dichloromaleic anhydride
Novikov,Balaneva,Shestak,Anufriev, V. Ph.,Glazunov
, p. 993 - 1003 (2017/01/11)
Under the drastic conditions of Zahn—Ochwat cycloacylation of 2-chloroand 2,3-dichlorohydroquinones with dichloromaleic anhydride (a melt of anhydrous AlCl3 and NaCl, 185—195 °C), the substrates undergo various degrees of disproportionation, which reduces the yields of the target triand tetrachloronaphthazarins. Quantum chemical calculations showed that the cycloacylation in question proceeds as a double aromatic electrophilic substitution of the vicinal protons with the corresponding oxocarbenium ions (acylium cations).
