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  2. methyl 2-[4-fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]acetate

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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)-

methyl 2-[4-fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]acetate

COC(=O)Cc1ccc(c(c1)B1OC(C(O1)(C)C)(C)C)F Request for Quotation
Chemical Name: methyl 2-[4-fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]acetate
CAS Number: 944317-66-2
Product Number: AG00II5Q(AGN-PC-07XUCY)
Synonyms:
MDL No:
Molecular Formula: C15H20BFO4
Molecular Weight: 294.1263

Identification/Properties

Computed Properties
Molecular Weight:
294.129g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
4
Exact Mass:
294.144g/mol
Monoisotopic Mass:
294.144g/mol
Topological Polar Surface Area:
44.8A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
383
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

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Chemical Structure


The Methyl 2-(4-fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetate is a versatile compound widely utilized in chemical synthesis. Specifically, it serves as a key building block in the synthesis of various complex organic molecules due to its unique structure and reactivity.This compound is particularly valuable in the formation of pharmaceutical intermediates, agrochemicals, and specialty chemicals. Its strategic positioning within the molecule allows for precise structural modifications, enabling chemists to introduce specific functional groups with high regioselectivity and stereoselectivity.Moreover, the presence of the boron-containing moiety enhances the compound's utility in Suzuki-Miyaura cross-coupling reactions, a powerful tool in carbon-carbon bond formation. This characteristic broadens the scope of synthetic routes available for the construction of intricate molecular architectures.Overall, the application of Methyl 2-(4-fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetate in chemical synthesis underscores its significance as a valuable synthetic building block, facilitating the efficient and selective assembly of diverse organic compounds.