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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)-

(3-chloro-4-hydroxy-5-methoxyphenyl)boronic acid

COc1cc(cc(c1O)Cl)B(O)O Request for Quotation
Chemical Name: (3-chloro-4-hydroxy-5-methoxyphenyl)boronic acid
CAS Number: 919496-57-4
Product Number: AG003BRV(AGN-PC-09PZ53)
Synonyms:
MDL No:
Molecular Formula: C7H8BClO4
Molecular Weight: 202.4000

Identification/Properties

Properties
MP:
158-160
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
202.397g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
202.02g/mol
Monoisotopic Mass:
202.02g/mol
Topological Polar Surface Area:
69.9A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
169
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

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Chemical Structure


(3-Chloro-4-hydroxy-5-methoxyphenyl)boronic acid is a versatile chemical compound commonly employed in chemical synthesis as a key building block. It serves as a valuable starting material for the preparation of various organic molecules due to its unique reactivity and structural properties.This boronic acid derivative is frequently used in Suzuki-Miyaura cross-coupling reactions, a powerful tool in modern organic chemistry for forming carbon-carbon bonds. By reacting with aryl halides or pseudohalides in the presence of a palladium catalyst, (3-Chloro-4-hydroxy-5-methoxyphenyl)boronic acid can be utilized to introduce the phenolic moiety into complex molecular structures.Moreover, the hydroxy and methoxy functional groups present in this compound offer additional avenues for further derivatization and modification. These functionalities can be leveraged to incorporate specific traits or properties into the final products, making it a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and materials science.Overall, (3-Chloro-4-hydroxy-5-methoxyphenyl)boronic acid plays a crucial role in enabling chemists to construct intricate organic frameworks efficiently and selectively, highlighting its significance in modern synthetic chemistry practices.