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  2. ethyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate

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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)-

ethyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate

CCOC(=O)c1ccc(cc1)B1OC(C(O1)(C)C)(C)C Request for Quotation
Chemical Name: ethyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate
CAS Number: 195062-62-5
Product Number: AG00APVS(AGN-PC-0KK6NF)
Synonyms:
MDL No:
Molecular Formula: C15H21BO4
Molecular Weight: 276.1358

Identification/Properties

Computed Properties
Molecular Weight:
276.139g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
276.153g/mol
Monoisotopic Mass:
276.153g/mol
Topological Polar Surface Area:
44.8A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
343
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#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Ethoxycarbonylphenylboronic acid pinacol ester is a versatile reagent commonly employed in organic chemical synthesis as a key building block. It serves as a valuable precursor in the preparation of various functionalized organic compounds through Suzuki-Miyaura cross-coupling reactions. This compound is particularly useful in the synthesis of biologically active molecules, pharmaceutical intermediates, and advanced materials. Its high reactivity and compatibility with a wide range of functional groups make it a valuable tool for chemists working in the field of organic synthesis.