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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)-

6-bromo-3-iodo-1H-pyrrolo[3,2-b]pyridine

Brc1cnc2c(c1)[nH]cc2I Request for Quotation
Chemical Name: 6-bromo-3-iodo-1H-pyrrolo[3,2-b]pyridine
CAS Number: 956485-60-2
Product Number: AG00H8NY(AGN-PC-04G0HB)
Synonyms:
MDL No:
Molecular Formula: C7H4BrIN2
Molecular Weight: 322.9285

Identification/Properties

Properties
BP:
392.4°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
322.931g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
321.86g/mol
Monoisotopic Mass:
321.86g/mol
Topological Polar Surface Area:
28.7A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
155
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
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-Bromo-3-iodo-1H-pyrrolo[3,2-b]pyridine is a valuable compound used in chemical synthesis for its unique properties and versatile applications. This heterocyclic compound is commonly employed as a key building block in the synthesis of complex organic molecules and pharmaceutical intermediates. By serving as a starting material in various reactions, 6-Bromo-3-iodo-1H-pyrrolo[3,2-b]pyridine enables the synthesis of novel compounds with diverse chemical structures and properties. Its presence in the chemical synthesis process allows for the introduction of specific functional groups and modifications that are crucial for the development of new materials, drugs, and agrochemicals. The strategic incorporation of 6-Bromo-3-iodo-1H-pyrrolo[3,2-b]pyridine in synthetic pathways facilitates the construction of intricate molecular architectures and enhances the efficiency and selectivity of chemical transformations. This compound plays a pivotal role in the innovative design and synthesis of advanced materials and bioactive molecules, making it an indispensable tool for organic chemists and researchers seeking to create novel compounds with tailored properties and applications.