1208076-70-3 Usage
General Description
2-Bromo-4-methylthiobenzamide is a chemical compound with the formula C8H8BrNOS. It is a white to light yellow solid that is commonly used in the production of pharmaceuticals and agrochemicals. 2-BROMO-4-METHYLTHIOBENZAMIDE is known for its ability to act as a selective and irreversible inhibitor of soluble epoxide hydrolase, an enzyme that plays a crucial role in regulating blood pressure and inflammation. Additionally, 2-Bromo-4-methylthiobenzamide is also utilized as an intermediate in the synthesis of various organic compounds, including dyes and pesticides. It is important to handle this chemical with caution, as it is considered to be harmful if swallowed or inhaled and can cause irritation to the skin and eyes.
Check Digit Verification of cas no
The CAS Registry Mumber 1208076-70-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,8,0,7 and 6 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1208076-70:
(9*1)+(8*2)+(7*0)+(6*8)+(5*0)+(4*7)+(3*6)+(2*7)+(1*0)=133
133 % 10 = 3
So 1208076-70-3 is a valid CAS Registry Number.
1208076-70-3Relevant articles and documents
Method for synthesizing thiobenzamide derivative through CO2 regulation and control of substituted benzonitrile
-
Paragraph 0037; 0038; 0040; 0041; 0042; 0049; 0051, (2019/01/24)
The invention discloses a method for synthesizing a thiobenzamide derivative through CO2 regulation and control of substituted benzonitrile. The method comprises the following steps: taking the substituted benzonitrile as a raw material, an inorganic sulfide as a sulfur source and CO2 as an auxiliary agent for reacting in the presence of a reaction solvent, and concentrating and purifying a reaction solution to obtain the thiobenzamide derivative. The reaction system disclosed by the invention is relatively simple, other catalysts are not added outside a reactant and the inorganic sulfide, themethod is suitable for synthesis of high-additional-value thiobenzamide containing a plurality of substituent groups, the reaction is carried out at low temperature and low pressure, and the risk coefficient is reduced.
