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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, 2'-deoxy-8-(phenylmethoxy)-

OC[C@H]1O[C@H](CC1O)n1c(OCc2ccccc2)nc2c1nc(N)[nH]c2=O Request for Quotation
Chemical Name: Guanosine, 2'-deoxy-8-(phenylmethoxy)-
CAS Number: 96964-90-8
Product Number: AG0065P9(AGN-PC-0OOII7)
Synonyms:
MDL No: MFCD03701133
Molecular Formula: C17H19N5O5
Molecular Weight: 373.3633

Identification/Properties

Properties
MP:
175-177°C
Storage:
2-8℃;
Computed Properties
Molecular Weight:
373.369g/mol
XLogP3:
0
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
5
Exact Mass:
373.139g/mol
Monoisotopic Mass:
373.139g/mol
Topological Polar Surface Area:
144A^2
Heavy Atom Count:
27
Formal Charge:
0
Complexity:
584
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
3
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


8-Benzyloxy-2'-deoxyguanosine is a versatile compound used in chemical synthesis as a protected form of deoxyguanosine. This compound is employed in nucleoside synthesis to introduce the guanosine base into oligonucleotides and nucleic acids. By utilizing 8-benzyloxy-2'-deoxyguanosine, chemists can selectively modify the position of the guanosine nucleobase while protecting the reactive groups of the molecule. This protection strategy allows for the precise control of reactions and the synthesis of complex nucleoside analogs with tailored properties.