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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)-

Pyridine, 4-[[[(1,1-dimethylethyl)dimethylsilyl]oxy]methyl]-

CC([Si](OCc1ccncc1)(C)C)(C)C Request for Quotation
Chemical Name: Pyridine, 4-[[[(1,1-dimethylethyl)dimethylsilyl]oxy]methyl]-
CAS Number: 117423-41-3
Product Number: AG000EAB(AGN-PC-0NE01Y)
Synonyms:
MDL No:
Molecular Formula: C12H21NOSi
Molecular Weight: 223.3867

Identification/Properties

Computed Properties
Molecular Weight:
223.391g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
4
Exact Mass:
223.139g/mol
Monoisotopic Mass:
223.139g/mol
Topological Polar Surface Area:
22.1A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
192
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#:
N/A
Hazard Statements:
H227-H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(((tert-Butyldimethylsilyl)oxy)methyl)pyridine is a versatile compound widely used in chemical synthesis due to its unique properties. It serves as an effective protecting group for alcohols in organic synthesis, where the tert-butyldimethylsilyl (TBDMS) group can be selectively removed under mild conditions. This compound finds application in the protection and deprotection of hydroxy functionalities, allowing for precise control over reactions and enabling the synthesis of complex molecules. The pyridine moiety enhances the solubility and stability of the compound, making it a valuable tool in organic chemistry for the synthesis of pharmaceuticals, natural products, and functional materials.