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  2. 1,3,2-Dioxaborolane,4,4,5,5-tetramethyl-2-[4-[2-(trimethylsilyl)ethynyl]phenyl]-

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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)-

1,3,2-Dioxaborolane,4,4,5,5-tetramethyl-2-[4-[2-(trimethylsilyl)ethynyl]phenyl]-

C[Si](C#Cc1ccc(cc1)B1OC(C(O1)(C)C)(C)C)(C)C Request for Quotation
Chemical Name: 1,3,2-Dioxaborolane,4,4,5,5-tetramethyl-2-[4-[2-(trimethylsilyl)ethynyl]phenyl]-
CAS Number: 870238-65-6
Product Number: AG008DVL(AGN-PC-0V9Z19)
Synonyms:
MDL No:
Molecular Formula: C17H25BO2Si
Molecular Weight: 300.2757

Identification/Properties

Computed Properties
Molecular Weight:
300.28g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
300.172g/mol
Monoisotopic Mass:
300.172g/mol
Topological Polar Surface Area:
18.5A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
428
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:
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


4,4,5,5-Tetramethyl-2-(4-trimethylsilanylethynyl-phenyl)-[1,3,2]dioxaborolane is a versatile compound widely used in chemical synthesis. This unique molecule plays a crucial role as a boron-containing building block in various organic reactions. In chemical synthesis, this compound acts as a valuable reagent for Suzuki-Miyaura cross-coupling reactions, which are fundamental transformations used to create carbon-carbon bonds. By serving as a boronic ester precursor, 4,4,5,5-Tetramethyl-2-(4-trimethylsilanylethynyl-phenyl)-[1,3,2]dioxaborolane facilitates the coupling of aryl and vinyl halides with aryl or alkenyl boronic acids. This reaction is of high importance in the synthesis of pharmaceuticals, agrochemicals, and materials science.Furthermore, the presence of the trimethylsilylethynyl group provides additional functionality, enabling further derivatization and diversification of the organic scaffold. This compound's compatibility with various functional groups and its stability under reaction conditions make it a valuable tool for chemists working in the field of organic synthesis.Overall, the incorporation of 4,4,5,5-Tetramethyl-2-(4-trimethylsilanylethynyl-phenyl)-[1,3,2]dioxaborolane in chemical synthesis offers a strategic advantage in the construction of complex molecules and the development of new materials with tailored properties.