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  2. 4,4,5,5-TETRAMETHYL-2-(3-TRIMETHYLSILANYLETHYNYL-PHENYL)-[1,3,2]DIOXABOROLANE

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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)-

4,4,5,5-TETRAMETHYL-2-(3-TRIMETHYLSILANYLETHYNYL-PHENYL)-[1,3,2]DIOXABOROLANE

C[Si](C#Cc1cccc(c1)B1OC(C(O1)(C)C)(C)C)(C)C Request for Quotation
Chemical Name: 4,4,5,5-TETRAMETHYL-2-(3-TRIMETHYLSILANYLETHYNYL-PHENYL)-[1,3,2]DIOXABOROLANE
CAS Number: 915402-03-8
Product Number: AG006L6G(AGN-PC-0WAG5I)
Synonyms:
MDL No:
Molecular Formula: C17H25BO2Si
Molecular Weight: 300.2757

Identification/Properties

Properties
MP:
86-90℃
Storage:
-10 ℃;
Form:
Solid
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:
436
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4,4,5,5-Tetramethyl-2-(3-trimethylsilanylethynyl-phenyl)-[1,3,2]dioxaborolane is a highly versatile compound widely used in chemical synthesis. One of its key applications is as a building block in organic synthesis, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. This compound serves as an efficient reagent for the introduction of boron-containing functional groups into various organic molecules, enabling the rapid and selective modification of complex structures. Additionally, 4,4,5,5-Tetramethyl-2-(3-trimethylsilanylethynyl-phenyl)-[1,3,2]dioxaborolane is utilized in the synthesis of pharmaceuticals, agrochemicals, and advanced materials due to its unique reactivity and compatibility with a wide range of functional groups. Its ability to facilitate diverse chemical transformations makes it an indispensable tool for researchers and chemists working in the field of organic synthesis.