1. Home
  2. Pyridine,3-iodo-2-(1-methylethoxy)-

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)-

Pyridine,3-iodo-2-(1-methylethoxy)-

CC(Oc1ncccc1I)C Request for Quotation
Chemical Name: Pyridine,3-iodo-2-(1-methylethoxy)-
CAS Number: 766557-61-3
Product Number: AG003JL7(AGN-PC-0UA7NE)
Synonyms:
MDL No:
Molecular Formula: C8H10INO
Molecular Weight: 263.0756

Identification/Properties

Properties
Storage:
Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
263.078g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
262.981g/mol
Monoisotopic Mass:
262.981g/mol
Topological Polar Surface Area:
22.1A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
119
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


3-Iodo-2-isopropoxypyridine is a versatile chemical compound that finds widespread application in organic synthesis. This compound serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and materials due to its unique structural properties.One key application of 3-Iodo-2-isopropoxypyridine lies in its use as a halogenated heterocyclic intermediate in the synthesis of biologically active compounds. By incorporating this molecule into a synthesis pathway, chemists can introduce specific functional groups and tailor the reactivity of the target molecule, allowing for precise control over the final product's properties.Furthermore, the presence of the iodo group in 3-Iodo-2-isopropoxypyridine enables nucleophilic substitution reactions, making it a valuable reagent for the modification of aromatic systems in complex molecules. This reactivity can be harnessed to introduce new substituents or scaffold modifications, expanding the chemical diversity and potential applications of the synthesized compounds.Overall, the strategic incorporation of 3-Iodo-2-isopropoxypyridine in chemical synthesis enables chemists to access novel structures and functionalities, driving innovation in drug discovery, materials science, and other fields that rely on the precise design and manipulation of organic molecules.