2812-86-4 Usage
Uses
Used in Pharmaceutical Industry:
2,4-Dichlorophenyl chlorothioformate is used as a reactant and intermediate for the synthesis of various pharmaceuticals. Its reactivity and versatility in organic synthesis make it a valuable component in the development of new drugs and medicinal compounds.
Used in Agrochemical Industry:
In the agrochemical sector, 2,4-Dichlorophenyl chlorothioformate is utilized as a reactant in the production of agrochemicals. Its role in the synthesis of these compounds contributes to the development of pesticides and other agricultural products designed to protect crops and enhance yields.
Used in Organic Compounds Synthesis:
Beyond its applications in pharmaceuticals and agrochemicals, 2,4-Dichlorophenyl chlorothioformate is also employed in the synthesis of a range of other organic compounds. Its chemical properties allow it to participate in various reactions, facilitating the creation of diverse organic molecules for different applications.
Environmental Considerations:
Given its potential as a groundwater contaminant and environmental pollutant, 2,4-Dichlorophenyl chlorothioformate necessitates proper handling and disposal methods. This is crucial to mitigate risks to human health and to preserve the integrity of the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 2812-86-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,1 and 2 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2812-86:
(6*2)+(5*8)+(4*1)+(3*2)+(2*8)+(1*6)=84
84 % 10 = 4
So 2812-86-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H3Cl3OS/c8-4-1-2-6(5(9)3-4)11-7(10)12/h1-3H
2812-86-4Relevant academic research and scientific papers
Constructing the OCF2O moiety using BrF3
Hagooly, Youlia,Rozen, Shlomo
, p. 6780 - 6783 (2008/12/22)
(Chemical Equation Presented) A general preparation for aromatic and aliphatic, cyclic as well as linear, symmetric and asymmetric difluoromethylenedioxy derivatives is described. The alcohols were reacted with thiophosgene to give thiocarbonates, which in turn were reacted with BrF 3. The fluorination step is complete in seconds with moderate to high yields under mild conditions.
