1. Home
  2. 4-Bromo-2-chlorophenylboronic acid

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-Bromo-2-chlorophenylboronic acid

Brc1ccc(c(c1)Cl)B(O)O Request for Quotation
Chemical Name: 4-Bromo-2-chlorophenylboronic acid
CAS Number: 1046861-20-4
Product Number: AG007GOM(AGN-PC-0WAA27)
Synonyms:
MDL No:
Molecular Formula: C6H5BBrClO2
Molecular Weight: 235.2707

Identification/Properties

Computed Properties
Molecular Weight:
235.268g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
233.925g/mol
Monoisotopic Mass:
233.925g/mol
Topological Polar Surface Area:
40.5A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
136
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


$Name$ is a highly versatile and valuable compound in the realm of chemical synthesis. As a boronic acid derivative with a unique (4-Bromo-2-chlorophenyl) substitution pattern, it plays a crucial role in organic reactions and pharmaceutical research. The presence of both bromine and chlorine atoms on the phenyl ring grants $Name$ a high degree of reactivity and specificity in various coupling reactions and cross-coupling processes. In the field of medicinal chemistry, (4-Bromo-2-chlorophenyl)boronic acid is widely utilized as a key building block for the synthesis of biologically active molecules, including pharmaceuticals and agrochemicals. Its ability to form stable boronate complexes with electrophiles makes it an indispensable tool for the creation of complex organic structures with precision and efficiency. The unique properties of (4-Bromo-2-chlorophenyl)boronic acid make it an essential component in the synthesis of novel compounds and the development of new drugs with potential therapeutic applications.