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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)-

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

O=Cc1cn(c2c1cccn2)S(=O)(=O)c1ccc(cc1)C Request for Quotation
Chemical Name: 1-(4-methylphenyl)sulfonylpyrrolo[2,3-b]pyridine-3-carbaldehyde
CAS Number: 956716-93-1
Product Number: AG005ZD3(AGN-PC-07CN65)
Synonyms:
MDL No:
Molecular Formula: C15H12N2O3S
Molecular Weight: 300.3324

Identification/Properties

Properties
BP:
530.109°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Tosyl-1H-pyrrolo[2,3-b]pyridine-3-carbaldehyde is a versatile compound widely used in chemical synthesis due to its unique reactivity and structural properties. Its application in organic chemistry primarily lies in its utility as a key building block for the synthesis of various heterocyclic compounds and pharmaceutical intermediates.This compound serves as an important starting material in the preparation of diverse complex molecules through its ability to participate in carbon-carbon and carbon-nitrogen bond-forming reactions. Its aldehyde group allows for selective functionalization, enabling the introduction of different substituents at specific positions in the molecule. Additionally, the tosyl group offers stability and can act as a protecting group during multi-step synthetic sequences.In particular, 1-Tosyl-1H-pyrrolo[2,3-b]pyridine-3-carbaldehyde finds significant use in the construction of bioactive molecules, such as antiviral agents, antibacterial compounds, and pharmaceuticals targeting various disease states. Its unique fused-ring structure imparts distinct chemical properties that make it valuable for accessing complex molecular architectures efficiently.Overall, the diverse synthetic applications of 1-Tosyl-1H-pyrrolo[2,3-b]pyridine-3-carbaldehyde make it a crucial tool in the arsenal of synthetic chemists for the construction of complex organic molecules with therapeutic potential.