AB46274
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
5g | 98% | in stock | $8.00 | $5.00 | - + | |
10g | 98% | in stock | $9.00 | $6.00 | - + | |
25g | 98% | in stock | $19.00 | $13.00 | - + | |
50g | 98% | in stock | $33.00 | $23.00 | - + | |
100g | 98% | in stock | $48.00 | $33.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AB46274 |
Chemical Name: | Indazole-3-carboxylic acid |
CAS Number: | 4498-67-3 |
Molecular Formula: | C8H6N2O2 |
Molecular Weight: | 162.1454 |
MDL Number: | MFCD00211066 |
SMILES: | OC(=O)c1n[nH]c2c1cccc2 |
NSC Number: | 520610 |
Complexity: | 196 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 12 |
Hydrogen Bond Acceptor Count: | 3 |
Hydrogen Bond Donor Count: | 2 |
Rotatable Bond Count: | 1 |
XLogP3: | 1.4 |
1H-Indazole-3-carboxylic acid is a versatile compound that finds significant application in chemical synthesis, particularly in the field of medicinal chemistry. It serves as a key building block for the synthesis of various biologically active molecules and pharmaceuticals due to its unique structural features and reactivity.One of the primary uses of 1H-Indazole-3-carboxylic acid is in the synthesis of indazole derivatives, which are important scaffolds in drug discovery and development. By functionalizing the carboxylic acid group or other positions on the indazole ring, chemists can introduce specific properties or functionalities into the final molecule, thereby modulating its biological activity or pharmacokinetic profile.Furthermore, 1H-Indazole-3-carboxylic acid can be utilized in the preparation of heterocyclic compounds, which are commonly found in bioactive molecules such as antibiotics, antivirals, and anticancer agents. The presence of the indazole moiety imparts favorable characteristics to the resulting compounds, making them promising candidates for further pharmacological evaluation.In summary, the strategic incorporation of 1H-Indazole-3-carboxylic acid into synthetic pathways enables chemists to access a diverse array of bioactive compounds with potential therapeutic applications. Its role in chemical synthesis underscores its importance in the development of new drug candidates and other valuable products in the pharmaceutical industry.
Chemical communications (Cambridge, England) 20121207
Bioorganic & medicinal chemistry letters 20120115
ChemMedChem 20120102
Reproduction (Cambridge, England) 20110501
Perspectives in medicinal chemistry 20110101
Physical chemistry chemical physics : PCCP 20090114
Bioorganic & medicinal chemistry 20081001
Medicina 20080101
Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501
Rapid communications in mass spectrometry : RCM 20050101
Reviews in urology 20050101
Drugs of today (Barcelona, Spain : 1998) 20030301
Biochemistry 20010206