1. Home
  2. 2,3-difluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

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)-

2,3-difluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

Fc1ncc(cc1F)B1OC(C(O1)(C)C)(C)C Request for Quotation
Chemical Name: 2,3-difluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
CAS Number: 1154579-82-4
Product Number: AG000G01(AGN-PC-09SIDK)
Synonyms:
MDL No:
Molecular Formula: C11H14BF2NO2
Molecular Weight: 241.0422

Identification/Properties

Computed Properties
Molecular Weight:
241.045g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
241.109g/mol
Monoisotopic Mass:
241.109g/mol
Topological Polar Surface Area:
31.4A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
285
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-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


The 2,3-Difluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is a versatile compound commonly used in chemical synthesis due to its unique properties. This compound serves as a valuable building block in organic chemistry, particularly in the field of medicinal chemistry and materials science. Its fluorinated structure provides enhanced stability and reactivity, making it a valuable tool for introducing fluorine atoms into complex molecules. In chemical synthesis, this compound is frequently employed as a key intermediate for the preparation of various pharmaceuticals, agrochemicals, and functional materials. Its strategic placement of functional groups allows for efficient derivatization and further modification, enabling the synthesis of diverse compounds with tailored properties. Additionally, the boron-containing moiety offers convenient handles for cross-coupling reactions, facilitating the formation of carbon-carbon and carbon-heteroatom bonds in complex molecular structures. Overall, the 2,3-Difluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine plays a crucial role in advancing the field of chemical synthesis by enabling the efficient construction of novel molecules with desired characteristics.