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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-1-methyl-

Cn1c(N)nc2c(c1=O)[nH]cn2 Request for Quotation
Chemical Name: 6H-Purin-6-one, 2-amino-1,7-dihydro-1-methyl-
CAS Number: 938-85-2
Product Number: AG00GT3Y(AGN-PC-0JL9M1)
Synonyms:
MDL No:
Molecular Formula: C6H7N5O
Molecular Weight: 165.1527

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Chemical Structure


1-Methylguanine, a derivative of guanine, plays a crucial role in chemical synthesis as a versatile building block. It serves as a key intermediate in the production of various pharmaceuticals, particularly anti-cancer drugs and antiviral agents. 1-Methylguanine is utilized in the synthesis of nucleoside analogs, which are essential components in the development of novel therapeutic agents targeting specific cellular processes. Additionally, this compound is employed in the creation of specialized nucleotide analogs for research purposes, enabling the study of DNA and RNA interactions and functions. Its unique structure and reactivity make 1-Methylguanine an indispensable tool in organic chemistry for the synthesis of biologically active compounds with diverse applications in the field of medicine and molecular biology.