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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)-

2,4,6-Tris(3,4-dichlorophenyl)boroxin

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Chemical Name: 2,4,6-Tris(3,4-dichlorophenyl)boroxin
CAS Number: 1133798-41-0
Product Number: AG008WOB(AGN-PC-0WAJDQ)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Computed Properties
Molecular Weight:
518.397g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
517.893g/mol
Monoisotopic Mass:
515.896g/mol
Topological Polar Surface Area:
27.7A^2
Heavy Atom Count:
30
Formal Charge:
0
Complexity:
495
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:
H302-H315-H320-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,4,6-Tris(3,4-dichlorophenyl)boroxin is a powerful and versatile compound frequently employed in modern chemical synthesis. Its unique structure, containing boron atoms bonded to multiple 3,4-dichlorophenyl groups, confers exceptional reactivity and selectivity in various reactions.This compound is widely used as a catalyst in organic transformations due to its Lewis acidic properties. In cross-coupling reactions, 2,4,6-tris(3,4-dichlorophenyl)boroxin can facilitate the formation of carbon-carbon bonds with high efficiency and control, leading to the rapid assembly of complex molecular structures. Additionally, it is a valuable reagent in Suzuki-Miyaura reactions, enabling the synthesis of biaryl compounds with high yields.Moreover, 2,4,6-Tris(3,4-dichlorophenyl)boroxin finds application in the construction of organoboron compounds, which are key intermediates in pharmaceutical and agrochemical synthesis. By serving as a boron source in various transformations, this boroxin derivative allows chemists to access diverse functional groups and stereochemistries in target molecules.Overall, the exceptional reactivity and catalytic properties of 2,4,6-Tris(3,4-dichlorophenyl)boroxin make it an indispensable tool for chemists engaged in innovative chemical synthesis strategies.