53078-70-9 Usage
General Description
2-Methoxy-5-methylbenzonitrile is an organic chemical compound that falls under the category of benzonitriles. Its molecular formula is C9H9NO and it is typically a light yellow colored liquid. Assessment of the compound reveals that it has a molecular weight of 147.18 g/mol. 2-Methoxy-5-methylbenzonitrile is distinguished by a nitrile group, or a carbon-nitrogen triple bond, and a methoxy group attached to the aromatic benzene ring. 2-Methoxy-5-methylbenzonitrile is used in research and is primarily part of laboratory settings. However, it can be hazardous and therefore, caution is required when handling it. It is usually kept in a cool, dry and well-ventilated place, and must be stored separately from oxidizing agents.
Check Digit Verification of cas no
The CAS Registry Mumber 53078-70-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,0,7 and 8 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 53078-70:
(7*5)+(6*3)+(5*0)+(4*7)+(3*8)+(2*7)+(1*0)=119
119 % 10 = 9
So 53078-70-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H9NO/c1-7-3-4-9(11-2)8(5-7)6-10/h3-5H,1-2H3
53078-70-9Relevant articles and documents
Facile one-pot transformation of arenes into aromatic nitriles under metal-cyanide-free conditions
Tamura, Toshiyuki,Moriyama, Katsuhiko,Togo, Hideo
, p. 2023 - 2029 (2015/03/18)
Electron-rich arenes bearing methyl or methoxy groups on the aromatic ring were treated with dichloromethyl methyl ether and ZnBr2, and then with molecular iodine and aq. ammonia to give the corresponding aromatic nitriles in good yields. Using this method, febuxostat was efficiently prepared from 4-bromophenol in four steps. The method can be used for the preparation of aromatic nitriles from arenes in one pot under metal-cyanide-free conditions. Various electron-rich arenes could be effectively converted into the corresponding aromatic nitriles in good yields, by treatment with ZnBr2 and dichloromethyl methyl ether, followed by reaction with molecular iodine and aq. ammonia.
