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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)-

1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-(2-naphthalenyl)-

CC1(C)OB(OC1(C)C)c1ccc2c(c1)cccc2 Request for Quotation
Chemical Name: 1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-(2-naphthalenyl)-
CAS Number: 256652-04-7
Product Number: AG003SQB(AGN-PC-0C5DU1)
Synonyms:
MDL No:
Molecular Formula: C16H19BO2
Molecular Weight: 254.1319

Identification/Properties

Properties
MP:
64.0 to 68.0 °C
BP:
378.7°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
254.136g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
254.148g/mol
Monoisotopic Mass:
254.148g/mol
Topological Polar Surface Area:
18.5A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
324
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#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The organic compound 1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-(2-naphthalenyl) is a versatile building block widely used in chemical synthesis. It serves as a valuable reagent in a variety of applications due to its unique structure and properties. In chemical synthesis, this compound is commonly employed as a boron source for Suzuki-Miyaura cross-coupling reactions. By serving as a boron reagent, it facilitates the formation of carbon-carbon bonds under mild reaction conditions, making it a valuable tool for the construction of complex organic molecules. Additionally, this compound is known to exhibit high stability and efficiency in these reactions, making it a preferred choice for researchers and synthetic chemists. Overall, the application of 1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-(2-naphthalenyl) in chemical synthesis offers a convenient and effective method for the synthesis of a wide range of organic compounds with diverse functionalities and applications.