7605-67-6 Usage
Uses
Used in Pharmaceutical Synthesis:
[1,1'-Biphenyl]-2-carboxylic acid, 2'-nitro-, methyl ester is used as an intermediate in the pharmaceutical industry for the synthesis of various drugs. Its unique structure allows for the creation of a wide range of medicinal compounds with potential therapeutic applications.
Used in Agrochemical Synthesis:
In the agrochemical industry, [1,1'-Biphenyl]-2-carboxylic acid, 2'-nitro-, methyl ester is utilized as a key intermediate in the development of pesticides and other agricultural chemicals. Its reactivity and structural features contribute to the production of effective and targeted agrochemical products.
Used in Organic Synthesis and Chemical Research:
Due to its distinctive structure and reactivity, [1,1'-Biphenyl]-2-carboxylic acid, 2'-nitro-, methyl ester may also find applications in the field of organic synthesis and chemical research. Researchers can leverage its properties to explore new reaction pathways and develop novel compounds with potential applications in various industries.
Safety and Handling:
It is crucial to handle [1,1'-Biphenyl]-2-carboxylic acid, 2'-nitro-, methyl ester with care, as it may present certain hazards and risks associated with its chemical properties. Proper safety measures, including the use of personal protective equipment and adherence to laboratory safety protocols, should be followed to minimize potential risks.
Check Digit Verification of cas no
The CAS Registry Mumber 7605-67-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,0 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7605-67:
(6*7)+(5*6)+(4*0)+(3*5)+(2*6)+(1*7)=106
106 % 10 = 6
So 7605-67-6 is a valid CAS Registry Number.
7605-67-6Relevant academic research and scientific papers
Diels-alder approach to biaryls: Elucidation of competing tandem [2+2] cycloaddition/[1,3] sigmatropic shift pathway
Ashburn, Bradley O.,Carter, Rich G.,Zakharov, Lev N.
experimental part, p. 7305 - 7309 (2009/05/09)
(Chemical Equation Presented) Reaction of 2-halo-6-nitrophenylacetylene with an electron deficient diene gives rise to a [4+2] cycloaddition/ cycloreversion biaryl product and a bicyclo[4.2.0]octadiene resulting from a competing [2+2] cycloaddition pathway. The cyclobutene can be opened to give a mixture of cyclooctatriene and biaryl in varying amounts depending on heat and light exposure. The conversion of the cyclobutene into biaryl occurs through a [1,3] sigmatropic carbon shift followed by [4+2] cycloextrusion of ethylene gas.
Synthesis of quinolines, 2-quinolones, phenanthridines, and 6(5H)-phenanthridinones via palladium[0]-mediated Ullmann cross-coupling of 1-bromo-2-nitroarenes with β-halo-enals, -enones, or -esters
Banwell, Martin G.,Lupton, David W.,Ma, Xinghua,Renner, Jens,Sydnes, Magne O.
, p. 2741 - 2744 (2007/10/03)
Palladium[0]-mediated Ullmann cross-coupling of 1-bromo-2-nitrobenzene (1 R = H) and its derivatives with a range of β-halo-enals, -enones, or -esters readily affords the corresponding β-aryl derivatives, which are converted into the corresponding quinolines, 2-quinolones, phenanthridines, or 6(5H)-phenanthridinones on reaction with dihydrogen in the presence of Pd on C or with TiCl3 in aqueous acetone.
