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  2. 1-phenyl-2-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]benzimidazole

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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-phenyl-2-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]benzimidazole

CC1(C)OB(OC1(C)C)c1cccc(c1)c1nc2c(n1c1ccccc1)cccc2 Request for Quotation
Chemical Name: 1-phenyl-2-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]benzimidazole
CAS Number: 952514-86-2
Product Number: AG00IIW6(AGN-PC-0C9RC0)
Synonyms:
MDL No:
Molecular Formula: C25H25BN2O2
Molecular Weight: 396.2892

Identification/Properties

Computed Properties
Molecular Weight:
396.297g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
396.201g/mol
Monoisotopic Mass:
396.201g/mol
Topological Polar Surface Area:
36.3A^2
Heavy Atom Count:
30
Formal Charge:
0
Complexity:
590
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-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Phenyl-2-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1H-benzo[d]imidazole serves as a valuable building block in chemical synthesis due to its versatility and unique structural features. This compound is commonly utilized as a key intermediate in the preparation of various organic molecules, particularly in the field of medicinal chemistry and materials science.In chemical synthesis, 1-Phenyl-2-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1H-benzo[d]imidazole can act as a precursor for the introduction of functional groups or substituents at specific positions in the molecular structure. Its strategic placement within a synthetic pathway allows for the efficient construction of complex molecules with desired properties.Furthermore, this compound plays a crucial role in cross-coupling reactions, such as Suzuki-Miyaura coupling, where it can participate as a boron-containing coupling partner to enable the formation of new carbon-carbon bonds. By incorporating 1-Phenyl-2-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1H-benzo[d]imidazole into synthetic routes, chemists can access a wide array of chemical structures and functionalized compounds for various applications.Overall, the versatile nature of 1-Phenyl-2-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1H-benzo[d]imidazole makes it a valuable tool in chemical synthesis, offering opportunities for innovation and creativity in the development of novel molecules and materials.