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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)-

2,4-dimethoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidine

COc1nc(OC)ncc1B1OC(C(O1)(C)C)(C)C Request for Quotation
Chemical Name: 2,4-dimethoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidine
CAS Number: 936250-17-8
Product Number: AG003FTH(AGN-PC-00UR19)
Synonyms:
MDL No:
Molecular Formula: C12H19BN2O4
Molecular Weight: 266.1013

Identification/Properties

Properties
BP:
397.4°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
266.104g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
3
Exact Mass:
266.144g/mol
Monoisotopic Mass:
266.144g/mol
Topological Polar Surface Area:
62.7A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
311
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


2,4-Dimethoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidine is a versatile compound widely utilized in chemical synthesis as a key building block for the construction of various functional molecules. In organic synthesis, this compound serves as an essential reagent for the formation of aromatic compounds, heterocycles, and pharmaceutical intermediates. Its unique structure imparts remarkable reactivity, allowing for efficient and selective transformations in complex chemical reactions. By incorporating 2,4-Dimethoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidine into synthetic pathways, chemists can achieve precise control over regioselectivity and stereoselectivity, facilitating the synthesis of diverse organic compounds with high purity and yield. This compound is indispensable for the development of novel materials, agrochemicals, and pharmaceuticals, making it a valuable tool in modern chemical research and innovation.