331-30-6 Usage
Description
N-(4-bromo-3-methylphenyl)acetamide is a chemical compound with the molecular formula C10H11BrNO. It is a derivative of acetamide, containing a 4-bromo-3-methylphenyl group attached to the nitrogen atom. N-(4-bromo-3-methylphenyl)acetamide is characterized by the presence of bromine and methyl groups in its structure, which can influence its stability and reactivity. It has been studied for its potential application in medicinal chemistry, particularly for its antimicrobial and analgesic properties.
Uses
Used in Pharmaceutical Synthesis:
N-(4-bromo-3-methylphenyl)acetamide is used as an intermediate in the synthesis of various pharmaceuticals and organic compounds. Its unique structure and reactivity make it a valuable building block for the development of new drugs and therapeutic agents.
Used in Medicinal Chemistry Research:
N-(4-bromo-3-methylphenyl)acetamide is used as a research compound in medicinal chemistry. Its antimicrobial and analgesic properties are of particular interest, as they may lead to the discovery of new treatments for bacterial infections and pain management.
Used in Organic Chemistry:
N-(4-bromo-3-methylphenyl)acetamide is also used in the field of organic chemistry, where its stability and reactivity are important factors in the development of new chemical reactions and processes. The presence of bromine and methyl groups in its structure makes it an important target for further research and development in this field.
Check Digit Verification of cas no
The CAS Registry Mumber 331-30-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,3 and 1 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 331-30:
(5*3)+(4*3)+(3*1)+(2*3)+(1*0)=36
36 % 10 = 6
So 331-30-6 is a valid CAS Registry Number.
331-30-6Relevant articles and documents
An Electrochemical Beckmann Rearrangement: Traditional Reaction via Modern Radical Mechanism
Tang, Li,Wang, Zhi-Lv,He, Yan-Hong,Guan, Zhi
, p. 4929 - 4936 (2020/08/21)
Abstract: Electrosynthesis as a potential means of introducing heteroatoms into the carbon framework is rarely studied. Herein, the electrochemical Beckmann rearrangement, i. e. the direct electrolysis of ketoximes to amides, is presented for the first time. Using a constant current as the driving force, the reaction can be easily carried out under neutral conditions at room temperature. Based on a series of mechanistic studies, a novel radical Beckmann rearrangement mechanism is proposed. This electrochemical Beckmann rearrangement does not follow the trans-migration rule of the classical Beckmann rearrangement.
HETEROCYCLIC INHIBITORS OF HISTAMINE RECEPTORS FOR THE TREATMENT OF DISEASE
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Page/Page column 99, (2011/10/05)
The present invention relates to compounds and methods which may be useful as inhibitors of H1R and/or H4R for the treatment or prevention of inflammatory, autoimmune, allergic, and ocular diseases.
A convenient synthesis of the potent mutagen 3,4,8-trimethyl-3H-imidazo[4,5-f]quinoxalin-2-amine.
Grivas
, p. 213 - 217 (2007/10/02)
The highly mutagenic title compound (4,8-DiMeIQx) was synthesized in 13% overall yield from 2-fluoro-5-nitrotoluene in eight operations. The average operation yield was 83%. The reaction sequence used gave, in addition to the title compound, the isomer 3,4,7-trimethyl-3H-imidazo[4,5-f]quinoxalin-2-amine (4,7-DiMeIQx).