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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)-

6-chloro-2-iodo-7H-purine

Ic1nc(Cl)c2c(n1)nc[nH]2 Request for Quotation
Chemical Name: 6-chloro-2-iodo-7H-purine
CAS Number: 18552-90-4
Product Number: AG00I1KD(AGN-PC-007KA1)
Synonyms:
MDL No:
Molecular Formula: C5H2ClIN4
Molecular Weight: 280.4537

Identification/Properties

Properties
MP:
218-220°C
BP:
582.2°C at 760 mmHg
Storage:
Inert atmosphere;-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
280.453g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
279.901g/mol
Monoisotopic Mass:
279.901g/mol
Topological Polar Surface Area:
54.5A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
157
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-Chloro-2-iodopurine is a versatile compound that finds wide application in chemical synthesis. As a halogenated purine derivative, it serves as a valuable building block in the preparation of various pharmaceuticals, agrochemicals, and advanced materials. In chemical synthesis, 6-Chloro-2-iodopurine is commonly used as a key intermediate for the synthesis of complex organic molecules. Its unique chemical structure and reactivity make it a valuable tool for introducing specific functional groups into target compounds. This compound can undergo various chemical transformations such as cross-coupling reactions, nucleophilic substitutions, and palladium-catalyzed reactions to create new bonds and modify molecular properties.Furthermore, the presence of both chlorine and iodine atoms in the molecular structure of 6-Chloro-2-iodopurine offers synthetic chemists the opportunity to fine-tune the physicochemical properties of the final products. The halogen atoms can impart specific characteristics such as electron density, lipophilicity, and reactivity, which are essential for designing molecules with desired pharmacological or biological activities.Overall, the strategic incorporation of 6-Chloro-2-iodopurine into synthetic pathways enables the efficient construction of complex molecules with tailored properties for a range of applications in drug discovery, material science, and chemical research.