847446-89-3 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
4-(3-Nitropyridin-2-yl)benzoic acid is used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals for its ability to contribute to the development of new drugs and pesticides. Its unique chemical structure allows for the creation of compounds with specific therapeutic or pesticidal properties.
Used in Antibacterial and Antifungal Applications:
4-(3-Nitropyridin-2-yl)benzoic acid is utilized as an antibacterial and antifungal agent due to its inherent properties that can combat bacterial and fungal infections. Its effectiveness in these applications is attributed to its chemical composition, which can interfere with the growth and survival of microorganisms.
Used in Materials Science:
In the field of materials science, 4-(3-Nitropyridin-2-yl)benzoic acid is employed as a building block in organic synthesis. Its structural features make it a valuable component in the development of new materials with specific properties, such as improved stability, reactivity, or selectivity.
Used as a Precursor in Chemical Production:
4-(3-Nitropyridin-2-yl)benzoic acid also serves as a precursor for the production of other chemicals, highlighting its importance in the synthesis of a wide range of compounds. Its role as a precursor allows for the creation of new chemical entities with diverse applications across various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 847446-89-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,7,4,4 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 847446-89:
(8*8)+(7*4)+(6*7)+(5*4)+(4*4)+(3*6)+(2*8)+(1*9)=213
213 % 10 = 3
So 847446-89-3 is a valid CAS Registry Number.
847446-89-3Relevant academic research and scientific papers
Biarylcarboxybenzamide derivatives as potent vanilloid receptor (VR1) antagonistic ligands
Park, Hyeung-Geun,Choi, Ji-Yeon,Kim, Mi-Hyun,Choi, Sea-Hoon,Park, Mi-Kyung,Lee, Jihye,Suh, Young-Ger,Cho, Hawon,Oh, Uhtaek,Kim, Hee-Doo,Joo, Yung Hyup,Shin, Song Seok,Kim, Jin Kwan,Jeong, Yeon Su,Koh, Hyun-Ju,Park, Young-Ho,Jew, Sang-Sup
, p. 631 - 634 (2007/10/03)
Seventeen biarylcarboxybenzamide derivatives were prepared for the study of their agonistic/antagonistic activities to the vanilloid receptor (VR1) in rat DRG neurons. The replacement of the piperazine moiety of the lead compound 1 with phenyl ring showed quite enhanced antagonistic activity. Among the prepared derivatives, N-(4-tert-butylphenyl)-4-pyridine-2-yl-benzamide (2, IC 50 = 31 nM) and N-(4-tert-butylphenyl)-4-(3-methylpyridine-2-yl) benzamide (3g, IC50 = 31 nM), showed 5-fold higher antagonistic activity than 1 in 45Ca2+-influx assay.
