113081-50-8 Usage
Description
2-(4-broMo-3-Methoxyphenyl)acetonitrile, also known as 4-Bromo-3-methoxyphenylacetonitrile, is a chemical compound characterized by the molecular formula C9H8BrNO. It is a nitrile derivative featuring a phenyl ring with a bromine atom and a methoxy group, attached alongside an acetonitrile functional group. 2-(4-broMo-3-Methoxyphenyl)acetonitrile is recognized for its role in organic synthesis and pharmaceutical research, primarily serving as a building block for the creation of various biologically active molecules. The unique chemical structure and properties of 2-(4-broMo-3-Methoxyphenyl)acetonitrile also suggest its potential in the development of innovative drugs and materials. However, caution is advised in its handling and application due to its potentially hazardous nature.
Uses
Used in Organic Synthesis:
2-(4-broMo-3-Methoxyphenyl)acetonitrile is utilized as a key intermediate in organic synthesis for the preparation of a range of chemical compounds. Its unique structure allows for versatile reactions, making it a valuable component in the synthesis of various organic molecules.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2-(4-broMo-3-Methoxyphenyl)acetonitrile serves as a building block for the development of biologically active compounds. Its presence in the molecular structure can influence the pharmacological properties of the resulting compounds, contributing to the discovery of new drugs with potential therapeutic applications.
Used in Drug Development:
2-(4-broMo-3-Methoxyphenyl)acetonitrile may also be employed in the development of new drugs, leveraging its chemical properties to enhance the efficacy and selectivity of medicinal agents. Its role in drug development could be crucial for creating novel therapeutics that address unmet medical needs.
Used in Material Science:
Given its unique chemical structure, 2-(4-broMo-3-Methoxyphenyl)acetonitrile may find applications in material science, potentially contributing to the creation of new materials with specialized properties for various industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 113081-50-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,0,8 and 1 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 113081-50:
(8*1)+(7*1)+(6*3)+(5*0)+(4*8)+(3*1)+(2*5)+(1*0)=78
78 % 10 = 8
So 113081-50-8 is a valid CAS Registry Number.
InChI:InChI=1S/C9H8BrNO/c1-12-9-6-7(4-5-11)2-3-8(9)10/h2-3,6H,4H2,1H3
113081-50-8Relevant articles and documents
COMPOUNDS AND THEIR METHODS OF USE
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, (2018/06/12)
The present invention is directed to, in part, fused heteroaryl compounds and compositions useful for preventing and/or treating a disease or condition relating to aberrant function of a voltage-gated, sodium ion channel, for example, abnormal late/persis
SUBSTITUTED FUSED BI- OR TRI- HETEROCYCLIC COMPOUNDS AS EHMT2 INHIBITORS
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Paragraph 0608; 0612; 0613; 0614, (2018/04/17)
The present disclosure relates to substituted fused bi- or tri- heterocyclic compounds. The present disclosure also relates to pharmaceutical compositions containing these compounds and methods of treating a disorder (e.g., sickle cell anemia) via inhibit
Oxidative aromatic C-O bond formation: synthesis of 3-functionalized benzo[b]furans by FeCl3-mediated ring closure of a-Aryl ketones
Liang, Zhidan,Hou, Weizhe,Du, Yunfei,Zhang, Yongliang,Pan, Yan,Mao, Deng,Zhao, Kang
supporting information; experimental part, p. 4978 - 4981 (2010/01/16)
A variety of 3-functionalized benzo[b]furans were achieved by way of a FeCl3-medlated Intramolecular cyclization of electron-rich a-aryl ketones. The alkoxy substituent on the benzene ring In the substrates was essential for an efficient cyclization to occur. This novel method allows the construction of benzo[b]furan rings by joining the O-atom on the side chain to the benzene ring via direct oxidative aromatic C-O bond formation.
