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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-(dimethylamino)-6-hydroxy-

CN(c1nc(O)cc(n1)O)C Request for Quotation
Chemical Name: 4(1H)-Pyrimidinone, 2-(dimethylamino)-6-hydroxy-
CAS Number: 5738-14-7
Product Number: AG00EDQ9(AGN-PC-0OCJPL)
Synonyms:
MDL No:
Molecular Formula: C6H9N3O2
Molecular Weight: 155.1546

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
155.157g/mol
XLogP3:
-0.9
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
155.069g/mol
Monoisotopic Mass:
155.069g/mol
Topological Polar Surface Area:
64.9A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
242
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

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(Dimethylamino)pyrimidine-4,6-diol plays a crucial role in chemical synthesis as a versatile building block. Its unique structure and properties make it an essential reagent for various reactions in organic chemistry. This compound is commonly used as a reagent in the synthesis of pharmaceuticals, agrochemicals, and other complex organic molecules. Due to its distinct electronic properties and reactivity, 2-(Dimethylamino)pyrimidine-4,6-diol serves as a valuable intermediate in the preparation of diverse chemical compounds. Its presence in the chemical synthesis process can facilitate the formation of new carbon-carbon and carbon-heteroatom bonds, enabling the creation of novel molecular structures with improved properties and functions.