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  2. 4,4,5,5-tetramethyl-2-(3-triphenylen-2-ylphenyl)-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-triphenylen-2-ylphenyl)-1,3,2-dioxaborolane

CC1(C)OB(OC1(C)C)c1cccc(c1)c1ccc2c(c1)c1ccccc1c1c2cccc1 Request for Quotation
Chemical Name: 4,4,5,5-tetramethyl-2-(3-triphenylen-2-ylphenyl)-1,3,2-dioxaborolane
CAS Number: 1115639-92-3
Product Number: AG008ZAY(AGN-PC-0CFCMI)
Synonyms:
MDL No:
Molecular Formula: C30H27BO2
Molecular Weight: 430.3452

Identification/Properties

Computed Properties
Molecular Weight:
430.354g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
430.21g/mol
Monoisotopic Mass:
430.21g/mol
Topological Polar Surface Area:
18.5A^2
Heavy Atom Count:
33
Formal Charge:
0
Complexity:
687
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:
H315-H319
Precautionary Statements:
P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4,4,5,5-Tetramethyl-2-(3-(triphenylen-2-yl)phenyl)-1,3,2-dioxaborolane is a versatile boron-containing compound that finds widespread applications in chemical synthesis. This unique compound serves as a valuable building block in the preparation of various organic molecules. Its boron moiety enables it to participate in important cross-coupling reactions, such as Suzuki-Miyaura coupling, a widely used method in the formation of carbon-carbon bonds.In chemical synthesis, 4,4,5,5-Tetramethyl-2-(3-(triphenylen-2-yl)phenyl)-1,3,2-dioxaborolane can be used to introduce specific functional groups or structural motifs into organic molecules. By reacting with suitable partner molecules under appropriate conditions, this compound facilitates the creation of complex molecular structures with improved yields and selectivity. Its unique molecular architecture, combining boron and aromatic groups, imparts special reactivity and selectivity characteristics that make it a valuable tool for organic chemists.The application of 4,4,5,5-Tetramethyl-2-(3-(triphenylen-2-yl)phenyl)-1,3,2-dioxaborolane in chemical synthesis extends to the synthesis of pharmaceuticals, agrochemicals, materials science, and other fields where precise control over molecular structure is essential. Its ability to participate in controlled reactions makes it a key player in modern synthetic chemistry, pushing the boundaries of what is achievable in the construction of intricate and functional organic molecules.