1. Home
  2. 3-iodo-1H-pyrrolo[2,3-c]pyridine

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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-1H-pyrrolo[2,3-c]pyridine

Ic1c[nH]c2c1ccnc2 Request for Quotation
Chemical Name: 3-iodo-1H-pyrrolo[2,3-c]pyridine
CAS Number: 956003-24-0
Product Number: AG00H8X0(AGN-PC-05SPIZ)
Synonyms:
MDL No:
Molecular Formula: C7H5IN2
Molecular Weight: 244.0325

Identification/Properties

Properties
BP:
380.5°C at 760 mmHg
Storage:
Light sensitive;Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
244.035g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
243.95g/mol
Monoisotopic Mass:
243.95g/mol
Topological Polar Surface Area:
28.7A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
129
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

Request for Quotation

Customer Feedback

Chemical Structure


3-Iodo-1H-pyrrolo[2,3-c]pyridine is a valuable organic compound widely utilized in chemical synthesis. One primary application of this compound is in the field of medicinal chemistry for the development of pharmaceuticals. Its unique structure and reactivity make it a versatile building block in the synthesis of various biologically active molecules.In the realm of organic synthesis, 3-Iodo-1H-pyrrolo[2,3-c]pyridine serves as a key intermediate in the construction of complex organic molecules. Its iodo-functional group allows for further derivatization through cross-coupling reactions, such as Suzuki and Heck couplings, enabling the introduction of various substituents to tailor the properties of the final product.Additionally, 3-Iodo-1H-pyrrolo[2,3-c]pyridine can be employed as a precursor in the synthesis of heterocyclic compounds, which are prevalent in pharmaceuticals, agrochemicals, and materials science. Its versatile nature makes it a valuable tool for chemists aiming to design and develop novel molecules with specific biological or physical properties.