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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)-

Pyrimidine, 2,4-bis[(trimethylsilyl)oxy]-

C[Si](Oc1ccnc(n1)O[Si](C)(C)C)(C)C Request for Quotation
Chemical Name: Pyrimidine, 2,4-bis[(trimethylsilyl)oxy]-
CAS Number: 10457-14-4
Product Number: AG007HH4(AGN-PC-0JLU0M)
Synonyms:
MDL No:
Molecular Formula: C10H20N2O2Si2
Molecular Weight: 256.4490

Identification/Properties

Computed Properties
Molecular Weight:
256.452g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
256.106g/mol
Monoisotopic Mass:
256.106g/mol
Topological Polar Surface Area:
44.2A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
226
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


2,4-Bis((trimethylsilyl)oxy)pyrimidine is a versatile compound that finds wide application in chemical synthesis as a powerful silylating agent. It is commonly utilized in organic chemistry reactions to selectively protect hydroxyl groups in various molecules. By forming trimethylsilyl ethers, this compound can prevent unwanted reactions or interactions with other functional groups during synthesis processes. Furthermore, 2,4-Bis((trimethylsilyl)oxy)pyrimidine enables the manipulation of molecules with hydroxyl groups, allowing for controlled modifications and enhancements in chemical structures. Its role in mediating selective transformations makes it a valuable tool in the synthesis of complex organic compounds and pharmaceutical intermediates.