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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)-

(2-bromo-6-ethoxyphenyl)boronic acid

CCOc1cccc(c1B(O)O)Br Request for Quotation
Chemical Name: (2-bromo-6-ethoxyphenyl)boronic acid
CAS Number: 957035-13-1
Product Number: AG003BLY(AGN-PC-0712PW)
Synonyms:
MDL No:
Molecular Formula: C8H10BBrO3
Molecular Weight: 244.8782

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
244.879g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
243.991g/mol
Monoisotopic Mass:
243.991g/mol
Topological Polar Surface Area:
49.7A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
156
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

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Chemical Structure


$Name$ is a versatile chemical compound known as (2-Bromo-6-ethoxyphenyl)boronic acid, which finds widespread application in the field of chemical synthesis. This unique boronic acid derivative serves as a crucial building block in the creation of various organic molecules and pharmaceutical compounds. In chemical synthesis, (2-Bromo-6-ethoxyphenyl)boronic acid acts as a key reagent for Suzuki-Miyaura cross-coupling reactions. This powerful reaction enables the formation of carbon-carbon bonds, essential for constructing complex organic structures. Furthermore, this compound is utilized in the preparation of organic materials, agrochemicals, and functional materials due to its exceptional reactivity and versatility in synthetic processes. With its significant role in advancing the realm of chemical synthesis, (2-Bromo-6-ethoxyphenyl)boronic acid is a valuable tool for chemists and researchers striving to develop innovative molecules and materials.