1. Home
  2. 4-Fluoro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

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-Fluoro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde

O=Cc1ccc(cc1B1OC(C(O1)(C)C)(C)C)F Request for Quotation
Chemical Name: 4-Fluoro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde
CAS Number: 1844839-22-0
Product Number: AG00I1GZ(AGN-PC-0WAMJP)
Synonyms:
MDL No: MFCD16996300
Molecular Formula: C13H16BFO3
Molecular Weight: 250.0737

Identification/Properties

Computed Properties
Molecular Weight:
250.076g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
250.118g/mol
Monoisotopic Mass:
250.118g/mol
Topological Polar Surface Area:
35.5A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
316
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


4-Fluoro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde is a versatile compound commonly used in chemical synthesis. Specifically, it serves as an important building block in organic chemistry due to its unique structural properties. This compound is frequently employed as a key intermediate in the synthesis of various pharmaceuticals, agrochemicals, and materials.One of the notable applications of 4-Fluoro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde is in the formation of carbon-carbon and carbon-heteroatom bonds through cross-coupling reactions. By utilizing palladium-catalyzed coupling methodologies, this compound can be reacted with a variety of nucleophiles to introduce fluorine atoms into complex organic molecules.Furthermore, 4-Fluoro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde is valued for its ability to selectively functionalize aromatic rings, facilitating the creation of novel chemical structures with specific properties. Its incorporation in organic synthesis processes enables chemists to access diverse molecular architectures efficiently and with high precision.Overall, the strategic use of 4-Fluoro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde in chemical synthesis provides a powerful tool for the construction of complex molecules with enhanced functionalities, making it a valuable component in the toolbox of synthetic chemists.