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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)-

Silanol, trimethyl-, lithium salt

C[Si](O)(C)C.[Li] Request for Quotation
Chemical Name: Silanol, trimethyl-, lithium salt
CAS Number: 2004-14-0
Product Number: AG002CQW(AGN-PC-0QRDIB)
Synonyms:
MDL No:
Molecular Formula: C3H10LiOSi
Molecular Weight: 97.1374

Identification/Properties

Computed Properties
Molecular Weight:
96.129g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
96.058g/mol
Monoisotopic Mass:
96.058g/mol
Topological Polar Surface Area:
23.1A^2
Heavy Atom Count:
6
Formal Charge:
0
Complexity:
32.3
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:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


Lithium trimethylsilanolate is a valuable reagent used in various chemical synthesis applications. This compound plays a crucial role in organic chemistry as a strong base and nucleophile. Its unique properties make it particularly useful in reactions where deprotonation and cross-coupling reactions are necessary. By serving as a strong base, lithium trimethylsilanolate can facilitate the formation of carbon-carbon and carbon-heteroatom bonds in complex organic molecules. Additionally, it is commonly employed in the preparation of silicon-containing compounds and in the synthesis of pharmaceuticals, agrochemicals, and materials science. With its versatile applications and reactivity profile, lithium trimethylsilanolate is an indispensable tool for synthetic chemists seeking efficient and selective transformations in their research and development endeavors.