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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-Bromomethyl-4-trifluoromethoxyphenylboronic acid, pinacol ester

BrCc1cc(ccc1B1OC(C(O1)(C)C)(C)C)OC(F)(F)F Request for Quotation
Chemical Name: 2-Bromomethyl-4-trifluoromethoxyphenylboronic acid, pinacol ester
CAS Number: 957066-13-6
Product Number: AG003GS3(AGN-PC-0WA6BI)
Synonyms:
MDL No:
Molecular Formula: C14H17BBrF3O3
Molecular Weight: 380.9932

Identification/Properties

Properties
Storage:
Room Temperature;
Computed Properties
Molecular Weight:
380.996g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
3
Exact Mass:
380.041g/mol
Monoisotopic Mass:
380.041g/mol
Topological Polar Surface Area:
27.7A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
387
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


2-(2-(Bromomethyl)-4-(trifluoromethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, commonly known as $name$, is a versatile compound frequently used in chemical synthesis. Its unique structure containing boron and halogen atoms makes it particularly valuable in a variety of synthetic applications.One of the key applications of $name$ in chemical synthesis is as a useful boron building block in Suzuki-Miyaura cross-coupling reactions. In this reaction, $name$ can act as the boron source, reacting with aryl halides or pseudohalides in the presence of a palladium catalyst to form biaryl compounds. This reaction is widely utilized in the synthesis of pharmaceuticals, agrochemicals, and materials science.Additionally, $name$ can also serve as a key intermediate in the construction of complex molecular architectures. Its trifluoromethoxy and bromomethyl substituents provide unique reactivity patterns, allowing for the introduction of these functional groups into target molecules with high selectivity and efficiency.Overall, the versatility and reactivity of 2-(2-(Bromomethyl)-4-(trifluoromethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane make it a valuable tool in modern chemical synthesis, enabling the efficient construction of novel compounds with diverse applications.