4067-82-7 Usage
Uses
Used in Pharmaceutical Industry:
Benzo[f]quinoline, 1-methyl-3-phenylis used as a precursor in the synthesis of various drugs. Its unique chemical structure allows it to be a key component in the development of new pharmaceuticals, contributing to the advancement of medicinal chemistry.
Used in Organic Compounds Synthesis:
Benzo[f]quinoline, 1-methyl-3-phenylis utilized as a building block in the synthesis of various organic compounds. Its aromatic properties and versatile chemical structure make it a valuable asset in the creation of complex organic molecules for a wide range of applications.
Used in Dye Production:
Benzo[f]quinoline, 1-methyl-3-phenylis used as a precursor in the production of dyes. Its aromatic nature and chemical composition contribute to the development of dyes with specific color properties and stability, making it an important compound in the dye industry.
Check Digit Verification of cas no
The CAS Registry Mumber 4067-82-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,6 and 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4067-82:
(6*4)+(5*0)+(4*6)+(3*7)+(2*8)+(1*2)=87
87 % 10 = 7
So 4067-82-7 is a valid CAS Registry Number.
4067-82-7Relevant academic research and scientific papers
Synthesis of New 3-Aryl-1-methylbenzo[f]quinolines
Kozlov,Basalaeva
, p. 718 - 722 (2007/10/03)
Three-component condensation of 2-aminonaphthalene, acetone, and substituted benzaldehydes in alcoholic solution in the presence of concentrated hydrochloric acid gave 3-aryl-1-methylbenzo[f]quinolines. 1-Methyl-3- (nitrophenyl)benzo[f]quinolines were reduced to the corresponding amines which were converted into amides having a sulfonyl or chloroacetyl group in the aryl substituent.
Synthesis of benzo[f]quinoline derivatives by condensation of arylmethylene-2-naphthylamines with ethyl acetoacetate
Kozlov,Sauts,Gusak
, p. 531 - 538 (2007/10/03)
Reaction of arylmethylene-2-naphthylamines with ethyl acetoacetate affords ethyl (3-arylbenzo-[f]quinol-1-yl)acetates. On boiling thereof with ethanol solutions of alkali arise the corresponding salts that when treated with mineral acids undergo decarboxylation to yield 3-aryl-1-methylbenzo[f]quinolines. Heating of ethyl (3-arylbenzo[f]quinol-1-yl)acetates with dimethyl sulfate gives rise to 3-aryl-4-methyl-1-ethoxycarbonylmethylbenzo[f]quinolinium methylsulfates which afford the corresponding perchlorates after treatment with HClO4.
