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  2. 4-chloro-3-iodo-1-(4-methylphenyl)sulfonylpyrrolo[2,3-b]pyridine

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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-1-(4-methylphenyl)sulfonylpyrrolo[2,3-b]pyridine

Cc1ccc(cc1)S(=O)(=O)n1cc(c2c1nccc2Cl)I Request for Quotation
Chemical Name: 4-chloro-3-iodo-1-(4-methylphenyl)sulfonylpyrrolo[2,3-b]pyridine
CAS Number: 869335-20-6
Product Number: AG008EHF(AGN-PC-09TA3G)
Synonyms:
MDL No:
Molecular Formula: C14H10ClIN2O2S
Molecular Weight: 432.6639

Identification/Properties

Computed Properties
Molecular Weight:
432.66g/mol
XLogP3:
4.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
431.92g/mol
Monoisotopic Mass:
431.92g/mol
Topological Polar Surface Area:
60.3A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
476
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


N-Tosyl-4-chloro-3-iodo-7-azaindole is a valuable compound in chemical synthesis, particularly in the field of medicinal chemistry. This versatile building block is commonly used in the development of pharmaceuticals and agrochemicals due to its unique structure and reactivity. Its strategic placement of chlorine and iodine atoms make it an important intermediate for the synthesis of various complex molecules.One of the key applications of N-Tosyl-4-chloro-3-iodo-7-azaindole is in the construction of heterocyclic compounds, which are essential components of many biologically active molecules. By incorporating this compound into a synthesis pathway, chemists can efficiently access diverse chemical structures with potential pharmacological activities. Additionally, the tosyl group in N-Tosyl-4-chloro-3-iodo-7-azaindole serves as a versatile handle for further functionalization, allowing for the introduction of various substituents to fine-tune the properties of the final compound.Overall, N-Tosyl-4-chloro-3-iodo-7-azaindole plays a crucial role in the synthesis of complex molecules with potential applications in drug discovery and agricultural chemistry. Its versatile nature and synthetic utility make it a valuable tool for chemists working in the field of organic synthesis.