88301-40-0 Usage
Description
2-Acetamido-4-bromoanisole is a chemical compound with the molecular formula C9H10BrNO2. It is a bromo-substituted anisole derivative, containing a bromine atom and an acetamido group. 2-Acetamido-4-bromoanisole has potential applications in various fields, including organic synthesis and pharmaceutical research.
Uses
Used in Pharmaceutical Research:
2-Acetamido-4-bromoanisole is used as a building block for the synthesis of pharmaceuticals and other bioactive molecules. Its unique chemical properties make it a valuable component in the development of new drugs and therapeutic agents.
Used in Organic Synthesis:
2-Acetamido-4-bromoanisole is used as a key intermediate in the synthesis of various organic compounds. Its versatility in chemical reactions allows for the creation of a wide range of molecules with different functional groups and properties.
Used in Research and Development:
2-Acetamido-4-bromoanisole is of interest to researchers and industries for its potential biological activities and applications. Its unique structure and properties make it a promising candidate for further study and development in various scientific and industrial fields.
Check Digit Verification of cas no
The CAS Registry Mumber 88301-40-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,3,0 and 1 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 88301-40:
(7*8)+(6*8)+(5*3)+(4*0)+(3*1)+(2*4)+(1*0)=130
130 % 10 = 0
So 88301-40-0 is a valid CAS Registry Number.
88301-40-0Relevant articles and documents
Method for preparing N-(3-acetyl-2-hydroxyphenyl)acetamide
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Paragraph 0036; 0042-0043; 0049; 0055-0056, (2019/07/04)
The invention relates to the technical field of organic synthesis and medicine, and provides a method for preparing N-(3-acetyl-2-hydroxyphenyl)acetamide. According to the method, 2-aminophenol is adopted as an initial raw material, amidogen acetylation and a methylation reaction of phenolic hydroxyl groups are firstly carried out, then bromination on benzene rings is carried out, acetyl is introduced, reductive debromination is finally carried out, a target product is obtained, and the total yield reaches up to 41.7%. In the process of generating a compound E through a compound D, the compound D is subjected to ether bond cracking, and can react with acetylchloride to generate phenolic ester, and then a rearrangement reaction occurs. According to the method, the raw material is wide in source and easy to obtain, the path can be industrialized easily, fewer impurities are generated, the yield is high, and the purity of the target product is effectively improved.
Para-Directed Amination of Electron-Rich Arenes with Bis(2,2,2-trichloroethyl) Azodicarboxylate
Leblanc, Yves,Boudreault, Nicolas
, p. 4268 - 4271 (2007/10/02)
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