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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, 2-iodo-3-methoxy-

COc1cccnc1I Request for Quotation
Chemical Name: Pyridine, 2-iodo-3-methoxy-
CAS Number: 93560-55-5
Product Number: AG00620A(AGN-PC-0JWHVG)
Synonyms:
MDL No:
Molecular Formula: C6H6INO
Molecular Weight: 235.0224

Identification/Properties

Properties
MP:
57-61°C
BP:
271.2°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Stability:
Light Sensitive
Computed Properties
Molecular Weight:
235.024g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
234.949g/mol
Monoisotopic Mass:
234.949g/mol
Topological Polar Surface Area:
22.1A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
89.1
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:
P233-P260-P261-P264-P270-P271-P280-P301+P312-P302+P352-P304-P304+P340-P305+P351+P338-P312-P321-P330-P332+P313-P337+P313-P340-P362-P403-P403+P233-P405-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Iodo-3-methoxypyridine is a valuable chemical compound used in various chemical synthesis processes. This versatile molecule plays a crucial role in organic chemistry as a key building block for the synthesis of pharmaceuticals, agrochemicals, and materials.In chemical synthesis, 2-Iodo-3-methoxypyridine is commonly employed as a nucleophilic reagent in reactions with electrophiles. Its iodo functional group enables it to participate in cross-coupling reactions, such as Suzuki-Miyaura and Stille couplings, leading to the formation of complex molecular structures. Additionally, the methoxy group can serve as a directing group, allowing for site-selective functionalization of aromatic systems.Furthermore, 2-Iodo-3-methoxypyridine can be utilized in heterocyclic chemistry for the construction of pyridine-containing compounds. By introducing this pyridine scaffold into molecules, chemists can modulate the properties and biological activities of the resulting products. This makes 2-Iodo-3-methoxypyridine an indispensable tool in the synthesis of pharmaceutical intermediates and bioactive compounds.Overall, the application of 2-Iodo-3-methoxypyridine in chemical synthesis underscores its importance in advancing organic chemistry research and facilitating the creation of novel molecules with diverse functionalities.