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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)-

2-Pyrimidinamine, 5-iodo-

Ic1cnc(nc1)N Request for Quotation
Chemical Name: 2-Pyrimidinamine, 5-iodo-
CAS Number: 1445-39-2
Product Number: AG001JNI(AGN-PC-0JOFUI)
Synonyms:
MDL No:
Molecular Formula: C4H4IN3
Molecular Weight: 220.9991

Identification/Properties

Computed Properties
Molecular Weight:
221.001g/mol
XLogP3:
0.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
220.945g/mol
Monoisotopic Mass:
220.945g/mol
Topological Polar Surface Area:
51.8A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
69.7
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-Amino-5-Iodopyrimidine is a versatile chemical compound that finds extensive application in organic synthesis. This compound serves as a key building block in the production of various pharmaceuticals, agrochemicals, and fine chemicals due to its unique structural properties and reactivity.In chemical synthesis, 2-Amino-5-Iodopyrimidine acts as a valuable intermediate for the preparation of heterocyclic compounds, which are crucial in drug discovery and development processes. It can be used as a precursor in the synthesis of biologically active molecules by participating in diverse reactions such as coupling reactions, nucleophilic substitutions, and cross-coupling reactions.Additionally, 2-Amino-5-Iodopyrimidine plays a significant role in the construction of complex organic molecules through the introduction of functional groups and structural modifications. Its selective reactivity towards specific functional groups makes it a desirable component in the synthesis of target compounds with high efficiency and precision.Overall, the application of 2-Amino-5-Iodopyrimidine in chemical synthesis facilitates the rapid and controlled generation of diverse chemical entities, making it an indispensable tool for organic chemists and researchers involved in the development of novel compounds with potential therapeutic or industrial applications.