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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-perylen-3-yl-1,3,2-dioxaborolane

CC1(C)OB(OC1(C)C)c1ccc2c3c1cccc3c1c3c2cccc3ccc1 Request for Quotation
Chemical Name: 4,4,5,5-tetramethyl-2-perylen-3-yl-1,3,2-dioxaborolane
CAS Number: 950761-81-6
Product Number: AG00IMKH(AGN-PC-04QMFQ)
Synonyms:
MDL No:
Molecular Formula: C26H23BO2
Molecular Weight: 378.2706

Identification/Properties

Computed Properties
Molecular Weight:
378.278g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
378.179g/mol
Monoisotopic Mass:
378.179g/mol
Topological Polar Surface Area:
18.5A^2
Heavy Atom Count:
29
Formal Charge:
0
Complexity:
629
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-(perylen-3-yl)-1,3,2-dioxaborolane is a highly versatile compound that finds wide application in chemical synthesis processes. This unique compound serves as a valuable building block in the formation of organic molecules with specific functionalities. Its unique structure, featuring the boron atom and perylene moiety, imparts distinct reactivity and properties that are beneficial in a variety of synthetic transformations.In chemical synthesis, 4,4,5,5-Tetramethyl-2-(perylen-3-yl)-1,3,2-dioxaborolane is commonly employed as a boronic acid derivative, allowing for the introduction of the perylene-3-yl group into a target molecule. This enables chemists to incorporate the distinctive properties of the perylene moiety into the final product, such as enhanced electronic properties or fluorescence characteristics. Additionally, the boron atom in the molecule can participate in various cross-coupling reactions, facilitating the formation of complex organic structures through C-C bond formation.Furthermore, the presence of multiple methyl groups in the molecule enhances its stability and solubility in organic solvents, making it a practical choice for use in a wide range of reaction conditions. Overall, 4,4,5,5-Tetramethyl-2-(perylen-3-yl)-1,3,2-dioxaborolane is an indispensable tool for synthetic chemists seeking to access novel organic compounds with tailored properties for applications in materials science, medicinal chemistry, and beyond.