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  2. 1H-Pyrrolo[2,3-b]pyridine, 1-[(4-methylphenyl)sulfonyl]-

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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)-

1H-Pyrrolo[2,3-b]pyridine, 1-[(4-methylphenyl)sulfonyl]-

Cc1ccc(cc1)S(=O)(=O)n1ccc2c1nccc2 Request for Quotation
Chemical Name: 1H-Pyrrolo[2,3-b]pyridine, 1-[(4-methylphenyl)sulfonyl]-
CAS Number: 348640-02-8
Product Number: AG00C6CA(AGN-PC-0K5T7M)
Synonyms:
MDL No:
Molecular Formula: C14H12N2O2S
Molecular Weight: 272.3223

Identification/Properties

Computed Properties
Molecular Weight:
272.322g/mol
XLogP3:
2.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
272.062g/mol
Monoisotopic Mass:
272.062g/mol
Topological Polar Surface Area:
60.3A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
410
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


1-Tosyl-1H-pyrrolo[2,3-b]pyridine is a versatile compound widely utilized in chemical synthesis due to its unique structural properties and reactivity. This heterocyclic compound serves as a valuable building block in the preparation of various complex organic molecules. Its incorporation into synthetic routes allows for the formation of diverse chemical structures with desirable properties. Specifically, 1-Tosyl-1H-pyrrolo[2,3-b]pyridine is commonly employed in the synthesis of pharmaceutical intermediates, agrochemicals, and advanced materials. By acting as a key intermediate in multi-step synthetic sequences, this compound enables the efficient construction of intricate molecular frameworks essential for the development of novel compounds in the fields of drug discovery and material science. Furthermore, the presence of the tosyl group enhances the compound's reactivity, facilitating its use in various transformations such as cross-coupling reactions and nucleophilic substitutions. Overall, the strategic incorporation of 1-Tosyl-1H-pyrrolo[2,3-b]pyridine in chemical synthesis enables the streamlined and effective assembly of complex molecules with diverse applications in research and industry.