1. Home
  2. Boronic acid, B-[4-(difluoromethoxy)-3,5-difluorophenyl]-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

Boronic acid, B-[4-(difluoromethoxy)-3,5-difluorophenyl]-

OB(c1cc(F)c(c(c1)F)OC(F)F)O Request for Quotation
Chemical Name: Boronic acid, B-[4-(difluoromethoxy)-3,5-difluorophenyl]-
CAS Number: 915401-97-7
Product Number: AG0036RI(AGN-PC-01LQW9)
Synonyms:
MDL No:
Molecular Formula: C7H5BF4O3
Molecular Weight: 223.9174

Identification/Properties

Properties
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
223.918g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
3
Exact Mass:
224.027g/mol
Monoisotopic Mass:
224.027g/mol
Topological Polar Surface Area:
49.7A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
195
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
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


The (4-(Difluoromethoxy)-3,5-difluorophenyl)boronic acid is a versatile compound widely utilized in chemical synthesis, particularly in the field of organic chemistry. Its unique properties make it a valuable tool for the creation of complex molecules and pharmaceuticals. This boronic acid derivative serves as a crucial building block in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds with high efficiency and selectivity. This reaction has become a fundamental technique in the synthesis of a broad range of organic compounds, including natural products, agrochemicals, and materials for various applications. The (4-(Difluoromethoxy)-3,5-difluorophenyl)boronic acid's ability to undergo such reactions opens up opportunities for chemists to design and assemble intricate molecular structures with precision and control. Its presence in the toolkit of synthetic chemists underscores its importance as a key component in advancing the frontiers of chemical research and development.