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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)-

Pyrimidine, 2-iodo-

Ic1ncccn1 Request for Quotation
Chemical Name: Pyrimidine, 2-iodo-
CAS Number: 31462-54-1
Product Number: AG00C6WU(AGN-PC-007GGV)
Synonyms:
MDL No:
Molecular Formula: C4H3IN2
Molecular Weight: 205.9845

Identification/Properties

Computed Properties
Molecular Weight:
205.986g/mol
XLogP3:
0.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
205.934g/mol
Monoisotopic Mass:
205.934g/mol
Topological Polar Surface Area:
25.8A^2
Heavy Atom Count:
7
Formal Charge:
0
Complexity:
51.7
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

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Chemical Structure


2-Iodopyrimidine is a versatile building block used in organic synthesis for the preparation of various functional molecules. It serves as a key starting material in the synthesis of pharmaceuticals, agrochemicals, and advanced materials due to its strategic position as a precursor in the construction of diverse chemical structures. With its unique reactivity and compatibility with a wide range of reactions, 2-Iodopyrimidine enables chemists to introduce specific functional groups and modify molecular scaffolds efficiently. Its applications in cross-coupling reactions, nucleophilic substitutions, and heterocycle synthesis highlight its importance in modern organic chemistry. By harnessing the synthetic potential of 2-Iodopyrimidine, researchers can access novel compounds with enhanced properties and potential applications across various industries.