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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-N-methyl-

OC[C@H]1O[C@H](C[C@@H]1O)n1cnc2c1nc(NC)[nH]c2=O Request for Quotation
Chemical Name: Guanosine, 2'-deoxy-N-methyl-
CAS Number: 19916-77-9
Product Number: AG002BXG(AGN-PC-0O6W5W)
Synonyms:
MDL No:
Molecular Formula: C11H15N5O4
Molecular Weight: 281.2679

Identification/Properties

Properties
MP:
>210°C (dec.)
Storage:
Keep in dry area;-10 ℃;Inert atmosphere;
Form:
Solid

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


2'-Deoxy-N2-methylguanosine is a valuable nucleoside derivative that finds wide application in chemical synthesis, particularly in the field of nucleic acid modification and medicinal chemistry. This compound serves as a versatile building block for the synthesis of modified oligonucleotides with enhanced stability and altered biological properties. By incorporating 2'-Deoxy-N2-methylguanosine into nucleic acid sequences, researchers can study the impact of specific modifications on base pairing, enzymatic stability, and gene expression. Additionally, this modified nucleoside can be utilized in the design of novel therapeutic agents targeting various diseases at the molecular level. In conclusion, 2'-Deoxy-N2-methylguanosine is a powerful tool for advancing research in nucleic acid biochemistry and drug development.