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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)-

Pyridine, 4-bromo-2-chloro-3-iodo-

Brc1ccnc(c1I)Cl Request for Quotation
Chemical Name: Pyridine, 4-bromo-2-chloro-3-iodo-
CAS Number: 916203-52-6
Product Number: AG006FM0(AGN-PC-067UDS)
Synonyms:
MDL No:
Molecular Formula: C5H2BrClIN
Molecular Weight: 318.3375

Identification/Properties

Properties
MP:
86-90℃
Storage:
2-8℃;Light sensitive;Inert atmosphere;
Form:
Solid
Computed Properties
Molecular Weight:
318.336g/mol
XLogP3:
3.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
316.81g/mol
Monoisotopic Mass:
316.81g/mol
Topological Polar Surface Area:
12.9A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
103
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:
Danger
UN#:
2811
Hazard Statements:
H301-H315-H319-H335
Precautionary Statements:
P261-P301+P310-P305+P351+P338
Class:
6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Bromo-2-chloro-3-iodopyridine is a versatile chemical compound commonly utilized in chemical synthesis processes. This compound serves as a valuable building block in the creation of complex organic molecules and pharmaceuticals due to its unique structural properties. In chemical synthesis, 4-Bromo-2-chloro-3-iodopyridine acts as a key intermediate for the preparation of a wide range of advanced compounds through various reactions such as cross-coupling, halogenation, and substitution reactions. Its selective halogenation pattern allows for precise control over the positioning of functional groups in the final products, making it an essential component in the development of new materials and bioactive compounds. Additionally, the presence of multiple halogen atoms in 4-Bromo-2-chloro-3-iodopyridine enhances its reactivity and compatibility with a variety of synthetic protocols, making it a highly sought-after reagent in the field of chemical synthesis.