20632-43-3 Usage
Uses
Used in Pharmaceutical Synthesis:
3-ABA is used as a key intermediate in the synthesis of pharmaceuticals, contributing to the development of new drugs and therapeutic agents. Its chemical structure allows for versatile modifications and functionalization, making it a valuable component in medicinal chemistry.
Used in Dye Production:
In the dye industry, 3-ABA serves as a precursor for the production of various dyes. Its chemical properties enable the creation of dyes with specific characteristics, such as color, stability, and solubility, which are essential for different applications.
Used in Biochemical Research:
3-ABA is widely employed as a biochemical reagent for the determination of reactive oxygen species (ROS). Its ability to react with ROS makes it a useful tool for studying oxidative stress and related biological processes in research settings.
Used in Cancer Therapy:
3-ABA has potential applications in cancer therapy, where it may be utilized in the development of targeted treatments or as a component of drug delivery systems. Its role in inhibiting the production of nitric oxide, a signaling molecule involved in various physiological and pathological processes, suggests its potential use in modulating cancer-related pathways.
Used in Imaging Techniques:
3-[(AMINOCARBONYL)AMINO]BENZOIC ACID's properties also lend itself to applications in imaging techniques, where it may be used as a contrast agent or in the development of imaging probes for visualizing biological processes or detecting diseases.
Overall, 3-[(Aminocarbonyl)amino]benzoic acid (3-ABA) is a versatile chemical compound with a range of applications across different industries, from pharmaceuticals and dyes to research and medical imaging. Its unique structure and properties make it a valuable asset in the development of new products and technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 20632-43-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,6,3 and 2 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 20632-43:
(7*2)+(6*0)+(5*6)+(4*3)+(3*2)+(2*4)+(1*3)=73
73 % 10 = 3
So 20632-43-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H8N2O3/c9-8(13)10-6-3-1-2-5(4-6)7(11)12/h1-4H,(H,11,12)(H3,9,10,13)
20632-43-3Relevant academic research and scientific papers
H-Bonding Assisted Self-Assembly of Anionic and Neutral Ligand on Metal: A Comprehensive Strategy to Mimic Ditopic Ligands in Olefin Polymerization
Mote, Nilesh R.,Patel, Ketan,Shinde, Dinesh R.,Gaikwad, Shahaji R.,Koshti, Vijay S.,Gonnade, Rajesh G.,Chikkali, Samir H.
supporting information, p. 12448 - 12456 (2017/10/24)
Self-assembly of two neutral ligands on a metal to mimic bidentate ligand coordination has been frequently encountered in the recent past, but self-assembly of an anionic ligand on a metal template alongside a neutral ligand remains an elusive target. Suc
RHO KINASE INHIBITORS
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Page/Page column 102, (2008/12/07)
Substituted amide and urea derivatives useful as inhibitors of Rho kinase are described, which inhibitors can be useful in the treatment of various disorders such as cardiovascular diseases, cancer, neurological diseases, renal diseases, bronchial asthma, erectile dysfunction and glaucoma.
Substituted benzene derivatives useful as neuraminidase inhibitors
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, (2008/06/13)
A compound of the Formula (I): STR1 or pharmaceutically-suitable salts or prodrug forms thereof, wherein: n is 0-1; m is 0; p is 0-1; R1 is --CO2 H; R2 is selected from the group consisting of H, --OH, and --NH2 ; R3 is H; R4 is --C(O)NHR8 ; R5 is --NHC(R6)NH2 R6 is selected from the group consisting of =NH, =NOH, =NCN, =O, and =S; and R8 is selected from the group consisting of C1 -C4 linear or branched alkyl substituted with 0-3 halogens on each carbon.
