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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)-

Carbonazidic acid, (4-methoxyphenyl)methyl ester

COc1ccc(cc1)COC(=O)N=[N+]=[N-] Request for Quotation
Chemical Name: Carbonazidic acid, (4-methoxyphenyl)methyl ester
CAS Number: 25474-85-5
Product Number: AG003LNH(AGN-PC-0JLLA4)
Synonyms:
MDL No:
Molecular Formula: C9H9N3O3
Molecular Weight: 207.18606

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Chemical Structure


The Carbonazidic acid, (4-methoxyphenyl)methyl ester is a versatile compound commonly used in chemical synthesis for its ability to facilitate various reactions. As a key reagent, it serves as a valuable building block in the synthesis of complex organic molecules. Its unique structure enables it to participate in a wide range of reactions, including nucleophilic substitution, condensation, and rearrangement processes. By incorporating this compound into reaction pathways, chemists can efficiently access new compounds with tailored properties and functionalities. In the realm of chemical synthesis, the Carbonazidic acid, (4-methoxyphenyl)methyl ester plays a crucial role in enabling the efficient and controlled construction of intricate molecular structures.