80021-34-7 Usage
Uses
Used in Organic Synthesis:
6-(3-Nitrophenyl)-picolinic acid is used as a building block in organic synthesis for the creation of various biologically active compounds. Its unique structure allows for the formation of complex organic molecules that can have potential applications in different fields.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 6-(3-Nitrophenyl)-picolinic acid is utilized as a key intermediate in the development of new drugs and pharmaceuticals. Its chemical properties enable the design and synthesis of novel therapeutic agents that can target specific biological pathways or diseases.
Used in Drug Development:
6-(3-Nitrophenyl)-picolinic acid is employed in drug development as a precursor to create pharmaceuticals with potential therapeutic benefits. Its reactivity and functional groups facilitate the synthesis of diverse drug candidates that can be further optimized for efficacy, safety, and other pharmaceutical properties.
Used in Chemical Research:
6-(3-Nitrophenyl)-picolinic acid is also used in chemical research to study the effects of nitro and phenyl groups on the chemical behavior of compounds. This can lead to a better understanding of molecular interactions and the development of new chemical reactions or processes.
Check Digit Verification of cas no
The CAS Registry Mumber 80021-34-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,0,2 and 1 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 80021-34:
(7*8)+(6*0)+(5*0)+(4*2)+(3*1)+(2*3)+(1*4)=77
77 % 10 = 7
So 80021-34-7 is a valid CAS Registry Number.
80021-34-7Relevant academic research and scientific papers
Antiallergic agents. 2. N-(1H-tetrazol-5-yl)-6-phenyl-2-pyridinecarboxamides
Honma,Oda,Hashiyama,Hanamoto,Nakai,Inoue,Ishida,Takeda,Ono,Tsuzurahara
, p. 1499 - 1504 (2007/10/02)
A new series of N-(1H-tetrazol-5-yl)-6-phenyl-2-pyridinecarboxamides was prepared to determine the effects of substituents on the benzene and pyridine rings on antiallergic activity in the rat passive cutaneous anaphylaxis (PCA) assay after oral administr
