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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)-

Guanosine, N-(phenoxyacetyl)-

OC[C@H]1O[C@H]([C@@H]([C@@H]1O)O)n1cnc2c1nc(NC(=O)COc1ccccc1)[nH]c2=O Request for Quotation
Chemical Name: Guanosine, N-(phenoxyacetyl)-
CAS Number: 119824-66-7
Product Number: AG01EAWO(AGN-PC-0NZYPA)
Synonyms:
MDL No:
Molecular Formula: C18H19N5O7
Molecular Weight: 417.37276

Identification/Properties

Computed Properties
Molecular Weight:
417.378g/mol
XLogP3:
0
Hydrogen Bond Donor Count:
5
Hydrogen Bond Acceptor Count:
9
Rotatable Bond Count:
6
Exact Mass:
417.128g/mol
Monoisotopic Mass:
417.128g/mol
Topological Polar Surface Area:
168A^2
Heavy Atom Count:
30
Formal Charge:
0
Complexity:
686
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
4
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


N-(2-Phenoxyacetyl)guanosine is a versatile compound used in chemical synthesis for its ability to modify nucleic acids. This compound is often utilized as a building block in the creation of modified nucleosides and oligonucleotides for various research and pharmaceutical applications. With its unique structure, N-(2-Phenoxyacetyl)guanosine can be incorporated into nucleic acid sequences to confer specific properties, such as enhanced stability or altered base pairing interactions. Additionally, this compound serves as a valuable tool in the development of novel nucleic acid-based therapeutics and diagnostic agents. In chemical synthesis, N-(2-Phenoxyacetyl)guanosine plays a crucial role in expanding the possibilities for designing and engineering nucleic acids with tailored functions and properties.