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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)-

3-iodo-4-methoxy-1H-pyrrolo[2,3-b]pyridine

COc1ccnc2c1c(I)c[nH]2 Request for Quotation
Chemical Name: 3-iodo-4-methoxy-1H-pyrrolo[2,3-b]pyridine
CAS Number: 928653-75-2
Product Number: AG0068A0(AGN-PC-04G0GH)
Synonyms:
MDL No:
Molecular Formula: C8H7IN2O
Molecular Weight: 274.0585

Identification/Properties

Properties
MP:
220-221°C
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
274.061g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
273.96g/mol
Monoisotopic Mass:
273.96g/mol
Topological Polar Surface Area:
37.9A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
167
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-H319
Precautionary Statements:
P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Iodo-4-methoxy-1H-pyrrolo[2,3-b]pyridine is a valuable building block in chemical synthesis, particularly in medicinal chemistry and drug development. This compound serves as a key intermediate in the synthesis of biologically active molecules due to its unique structural features and reactivity. One prominent application of 3-Iodo-4-methoxy-1H-pyrrolo[2,3-b]pyridine is in the construction of heterocyclic compounds, which are prevalent in pharmaceuticals and agrochemicals. By incorporating this moiety into organic molecules, chemists can modulate their properties and enhance their biological activities. Additionally, the presence of the iodo and methoxy groups in 3-Iodo-4-methoxy-1H-pyrrolo[2,3-b]pyridine offers synthetic versatility, allowing for further elaboration and functionalization to generate diverse chemical entities with desired pharmacological profiles. This compound plays a crucial role in expanding the chemical space for drug discovery and development, making it a valuable tool for organic chemists striving to create novel therapeutics and research compounds.