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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, 9-[[2-(acetyloxy)ethoxy]methyl]-2-amino-1,9-dihydro-

CC(=O)OCCOCn1cnc2c1nc(N)[nH]c2=O Request for Quotation
Chemical Name: 6H-Purin-6-one, 9-[[2-(acetyloxy)ethoxy]methyl]-2-amino-1,9-dihydro-
CAS Number: 102728-64-3
Product Number: AG000885(AGN-PC-0NVG4Y)
Synonyms:
MDL No:
Molecular Formula: C10H13N5O4
Molecular Weight: 267.2413

Identification/Properties

Computed Properties
Molecular Weight:
267.245g/mol
XLogP3:
-1.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
6
Exact Mass:
267.097g/mol
Monoisotopic Mass:
267.097g/mol
Topological Polar Surface Area:
121A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
399
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

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Chemical Structure


The compound 2-((2-Amino-6-oxo-1H-purin-9(6H)-yl)methoxy)ethyl acetate plays a crucial role in chemical synthesis due to its structural properties and reactivity. This compound serves as an important building block in the creation of various pharmaceutical agents, nucleoside analogs, and other organic compounds.In chemical synthesis, 2-((2-Amino-6-oxo-1H-purin-9(6H)-yl)methoxy)ethyl acetate can be utilized as a masked form of a purine nucleoside. The presence of the amino and carbonyl groups in the molecule allows for selective functionalization and modification, making it a versatile intermediate in the synthesis of complex organic molecules.Furthermore, the acetate group in the compound provides protection for the amino group, allowing for controlled deprotection reactions during the synthesis process. This protective group strategy enables chemists to perform specific reactions at desired positions on the molecule, leading to the efficient and targeted synthesis of various compounds.Overall, the application of 2-((2-Amino-6-oxo-1H-purin-9(6H)-yl)methoxy)ethyl acetate in chemical synthesis demonstrates its importance as a key intermediate in the construction of biologically active molecules and functional materials.