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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

4-Chloro-3-iodo-1H-pyrazolo[3,4-b]pyridine

Clc1ccnc2c1c(I)n[nH]2 Request for Quotation
Chemical Name: 4-Chloro-3-iodo-1H-pyrazolo[3,4-b]pyridine
CAS Number: 949558-30-9
Product Number: AG005U1X(AGN-PC-0WAI6B)
Synonyms:
MDL No:
Molecular Formula: C6H3ClIN3
Molecular Weight: 279.4656

Identification/Properties

Properties
BP:
390.8°C at 760 mmHg
Storage:
2-8℃;Light sensitive;
Form:
Solid
Computed Properties
Molecular Weight:
279.465g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
278.906g/mol
Monoisotopic Mass:
278.906g/mol
Topological Polar Surface Area:
41.6A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
157
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Chloro-3-iodo-1H-pyrazolo[3,4-b]pyridine is a versatile compound widely used in chemical synthesis as a key intermediate in the production of various pharmaceuticals, agrochemicals, and functional materials. Its unique structure and reactivity make it a valuable building block for synthesizing heterocyclic compounds with diverse applications.In chemical synthesis, 4-Chloro-3-iodo-1H-pyrazolo[3,4-b]pyridine acts as a nucleophilic halogenation agent, allowing for the introduction of chlorine and iodine functionalities into complex molecular frameworks. This compound serves as a key component in the construction of biologically active molecules, such as kinase inhibitors, antibacterial agents, and antiviral drugs.Furthermore, the presence of both chlorine and iodine atoms in 4-Chloro-3-iodo-1H-pyrazolo[3,4-b]pyridine confers enhanced chemical diversity and pharmacological properties to the synthesized compounds. Its strategic incorporation in multistep synthesis processes enables the formation of structurally complex compounds with improved efficacy and selectivity.Overall, the application of 4-Chloro-3-iodo-1H-pyrazolo[3,4-b]pyridine in chemical synthesis facilitates the efficient and cost-effective production of novel compounds with valuable biological activities and potential for further exploration in drug discovery and materials science.