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  2. 4(1H)-Pyrimidinone, 2-amino-5-[(3,4,5-trimethoxyphenyl)methyl]-

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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)-

4(1H)-Pyrimidinone, 2-amino-5-[(3,4,5-trimethoxyphenyl)methyl]-

COc1cc(Cc2c[nH]c(nc2=O)N)cc(c1OC)OC Request for Quotation
Chemical Name: 4(1H)-Pyrimidinone, 2-amino-5-[(3,4,5-trimethoxyphenyl)methyl]-
CAS Number: 92440-76-1
Product Number: AG00GXCK(AGN-PC-0ON7FE)
Synonyms:
MDL No:
Molecular Formula: C14H17N3O4
Molecular Weight: 291.30248

Identification/Properties

Computed Properties
Molecular Weight:
291.307g/mol
XLogP3:
0.5
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
5
Exact Mass:
291.122g/mol
Monoisotopic Mass:
291.122g/mol
Topological Polar Surface Area:
95.2A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
436
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
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


2-Amino-5-[(3,4,5-trimethoxyphenyl)methyl]-4(3H)-pyrimidinone plays a crucial role in chemical synthesis as a versatile building block. Its unique molecular structure allows for the creation of various organic compounds through sequential reactions. In particular, this compound has been utilized in the synthesis of bioactive molecules and pharmaceutical drugs. Its presence as a key intermediate enables the formation of complex structures with high efficiency, making it a valuable tool in the synthesis of novel chemical entities with potential therapeutic applications.