62530-49-8 Usage
Description
2-(3-Carboxyprop-2-enoylamino)benzoic acid is a chemical compound with the molecular formula C13H11NO5. It is a derivative of benzoic acid and contains a carboxylic acid group and an enoylamine group. 2-(3-CARBOXYPROP-2-ENOYLAMINO)BENZOIC ACID is known for its potential antimicrobial and anti-inflammatory properties, as well as its potential use in the treatment of various diseases such as cancer and diabetes.
Uses
Used in Pharmaceutical Industry:
2-(3-Carboxyprop-2-enoylamino)benzoic acid is used as an active pharmaceutical ingredient for its antimicrobial and anti-inflammatory properties. It is employed in the development of drugs that target bacterial infections and inflammatory conditions.
Used in Cancer Treatment:
In the field of oncology, 2-(3-Carboxyprop-2-enoylamino)benzoic acid is used as a potential therapeutic agent for the treatment of various types of cancer. Its mechanism of action may involve targeting specific cellular pathways or processes that contribute to tumor growth and progression.
Used in Diabetes Management:
2-(3-Carboxyprop-2-enoylamino)benzoic acid is also being studied for its potential role in the management of diabetes. It may help regulate blood sugar levels or improve insulin sensitivity, contributing to better diabetes control.
Used as a Building Block in Synthesis:
In the synthesis of other pharmaceutical compounds, 2-(3-Carboxyprop-2-enoylamino)benzoic acid serves as a valuable building block. Its unique structure allows it to be incorporated into the development of new drugs with diverse therapeutic applications.
Used in Research and Development:
2-(3-Carboxyprop-2-enoylamino)benzoic acid is utilized in research and development settings to explore its potential applications in various therapeutic areas. Scientists investigate its properties and interactions with biological systems to uncover new possibilities for its use in medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 62530-49-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,5,3 and 0 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 62530-49:
(7*6)+(6*2)+(5*5)+(4*3)+(3*0)+(2*4)+(1*9)=108
108 % 10 = 8
So 62530-49-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H9NO5/c13-9(5-6-10(14)15)12-8-4-2-1-3-7(8)11(16)17/h1-6H,(H,12,13)(H,14,15)(H,16,17)/b6-5-
62530-49-8Relevant articles and documents
The synthesis of (Z)-4-oxo-4-(arylamino)but-2-enoic acids derivatives and determination of their inhibition properties against human carbonic anhydrase I and II isoenzymes
Oktay, Koray,K?se, Leyla Polat,?endil, K?v?lc?m,Gültekin, Mehmet Serdar,Gül?in, ?lhami,Supuran, Claudiu T.
, p. 939 - 945 (2016/10/09)
The synthesis of (Z)-4-oxo-4-(arylamino)but-2-enoic acid (4) derivatives containing structural characteristics that can be used for the synthesis of several active molecules, is presented. Some of the butenoic acid derivatives (4a, 4c, 4e, 4i, 4j, 4k) are
1H and 13C NMR spectra for a series of arylmaleamic acids, arylmaleimides, arylsuccinamic acids and arylsuccinimides
Trujillo-Ferrara, Jose,Santillan, Rosa,Beltran, Hiram I.,Farfan, Norberto,Hoepfl, Herbert
, p. 682 - 686 (2007/10/03)
The 1H and 13C NMR spectra of 17 succinic anhydride derivatives and 25 maleic anhydride derivatives were completely assigned using one- and two-dimensional NMR techniques. Copyright
Ortho Substituent Effects in Amide Hydrolysis of Maleanilic Acid Derivatives. Stabilization of Positive Charge Developed in the Transition State
Suh, Junghun,Kim, Mahn Joo,Kim, Chong Bok
, p. 2453 - 2456 (2007/10/02)
The effects of ortho substituents on the rate of the hydrolysis of maleanilic acid derivatives have been studied.The rate is enhanced up to 55 times by polar substituents, while it is retarded greatly by nonpolar substituents.The acceleration by the polar
