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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)-

Boronic acid, (5-chloro-2-methoxyphenyl)-

COc1ccc(cc1B(O)O)Cl Request for Quotation
Chemical Name: Boronic acid, (5-chloro-2-methoxyphenyl)-
CAS Number: 89694-48-4
Product Number: AG00348W(AGN-PC-0KK7BK)
Synonyms:
MDL No: MFCD01318966
Molecular Formula: C7H8BClO3
Molecular Weight: 186.4006

Identification/Properties

Properties
MP:
134-141 °C(lit.)
BP:
360.2 °C at 760 mmHg
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
186.398g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
186.026g/mol
Monoisotopic Mass:
186.026g/mol
Topological Polar Surface Area:
49.7A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
145
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


5-Chloro-2-methoxyphenylboronic acid is a versatile compound widely used in chemical synthesis as a key building block in the preparation of various organic molecules. This compound serves as a crucial reagent in Suzuki coupling reactions, a powerful method for forming carbon-carbon bonds. By reacting 5-Chloro-2-methoxyphenylboronic acid with suitable partner molecules in the presence of a palladium catalyst, chemists can efficiently construct complex structures with precise control over the connecting carbon-carbon bonds.Additionally, this compound can participate in other important reactions such as cross-coupling, arylation, and heterocycle synthesis, enabling the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its unique structure and reactivity make it a valuable tool for organic chemists seeking to streamline their synthetic routes and access diverse chemical space efficiently.