1H-Pyrazolo[3,4-b]pyridine-1-carboxylic acid, 3-iodo-, 1,1-dimethylethylester


Chemical Name: 1H-Pyrazolo[3,4-b]pyridine-1-carboxylic acid, 3-iodo-, 1,1-dimethylethylester
CAS Number: 920036-34-6
Product Number: AG00IGZO(AGN-PC-0VXQQ4)
Synonyms:
MDL No:
Molecular Formula: C11H12IN3O2
Molecular Weight: 345.1363

Identification/Properties


Computed Properties
Molecular Weight:
345.14g/mol
XLogP3:
2.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
344.997g/mol
Monoisotopic Mass:
344.997g/mol
Topological Polar Surface Area:
57A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
306
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum


Other Analytical Data


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Chemical Structure



The tert-Butyl 3-iodo-1H-pyrazolo[3,4-b]pyridine-1-carboxylate, often utilized in chemical synthesis, serves as a significant building block in the creation of various organic compounds. This compound plays a crucial role in the synthesis of complex heterocyclic structures, particularly in medicinal chemistry and drug development. Its unique chemical properties enable it to facilitate the formation of innovative molecular structures with diverse functionalities, making it a valuable tool for researchers and chemists in the field. Its application in chemical synthesis contributes to the advancement of pharmaceuticals, agrochemicals, and materials science, showcasing its versatility and importance in modern organic synthesis strategies.