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  2. 6H-Purin-6-one, 2-amino-1,7-dihydro-7-[(2-hydroxyethoxy)methyl]-

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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)-

6H-Purin-6-one, 2-amino-1,7-dihydro-7-[(2-hydroxyethoxy)methyl]-

OCCOCn1cnc2c1c(=O)[nH]c(n2)N Request for Quotation
Chemical Name: 6H-Purin-6-one, 2-amino-1,7-dihydro-7-[(2-hydroxyethoxy)methyl]-
CAS Number: 91702-61-3
Product Number: AG00GWHD(AGN-PC-0OMW6T)
Synonyms:
MDL No:
Molecular Formula: C8H11N5O3
Molecular Weight: 225.20464

Identification/Properties

Properties
MP:
271 - 273ºC
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
225.208g/mol
XLogP3:
-1.9
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
4
Exact Mass:
225.086g/mol
Monoisotopic Mass:
225.086g/mol
Topological Polar Surface Area:
115A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
308
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


2-Amino-7-((2-hydroxyethoxy)methyl)-1H-purin-6(7H)-one, commonly known as $name$, is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. In organic synthesis, $name$ serves as a key intermediate for the preparation of various biologically active molecules, pharmaceuticals, and functional materials.One of the main applications of $name$ in chemical synthesis is its utility as a building block for the synthesis of nucleoside analogs. By modifying the purine ring system or the side chain attached to the amino group, chemists can tailor the structure of the final nucleoside analog to impart specific biological activities or properties. This makes $name$ an invaluable starting material for the development of new antiviral, anticancer, or antifungal agents.Furthermore, the hydroxyethoxy side chain in $name$ provides a versatile functional group that can undergo various chemical transformations, such as esterification, etherification, oxidation, or reduction. These reactions allow for the introduction of additional substituents or modifications to the molecule, expanding the library of compounds that can be synthesized using $name$ as a precursor.Overall, the strategic placement of the amino group, hydroxyethoxy moiety, and purine ring scaffold in $name$ make it a valuable reagent for the synthesis of diverse organic compounds with potential applications in medicinal chemistry, materials science, and drug discovery.