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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-(benzenesulfonyl)-4-chloro-2-iodopyrrolo[2,3-b]pyridine

Clc1ccnc2c1cc(n2S(=O)(=O)c1ccccc1)I Request for Quotation
Chemical Name: 1-(benzenesulfonyl)-4-chloro-2-iodopyrrolo[2,3-b]pyridine
CAS Number: 940948-30-1
Product Number: AG00GTY5(AGN-PC-072DBE)
Synonyms:
MDL No:
Molecular Formula: C13H8ClIN2O2S
Molecular Weight: 418.6373

Identification/Properties

Computed Properties
Molecular Weight:
418.633g/mol
XLogP3:
3.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
417.904g/mol
Monoisotopic Mass:
417.904g/mol
Topological Polar Surface Area:
60.3A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
450
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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Chloro-2-iodo-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine is a versatile compound that finds valuable application in chemical synthesis. This compound is commonly utilized as a key building block in the creation of complex organic molecules due to its unique structure and reactivity.In chemical synthesis, 4-Chloro-2-iodo-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine serves as an important intermediate for the construction of various heterocyclic compounds. Its presence in a synthetic pathway allows for the introduction of structural diversity and functional groups, facilitating the creation of novel molecules with specific properties and functionalities.Furthermore, the strategic placement of the chloro, iodo, and phenylsulfonyl groups on the pyrrolo[2,3-b]pyridine scaffold enables precise manipulation of its chemical reactivity, enabling chemists to perform diverse transformations such as cross-coupling reactions, nucleophilic substitutions, and metal-mediated reactions.Overall, the use of 4-Chloro-2-iodo-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine in chemical synthesis offers a valuable tool for the construction of complex organic molecules with tailored structures and properties.