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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, (4-chloro-3-hydroxyphenyl)-

OB(c1ccc(c(c1)O)Cl)O Request for Quotation
Chemical Name: Boronic acid, (4-chloro-3-hydroxyphenyl)-
CAS Number: 915201-06-8
Product Number: AG003L4V(AGN-PC-07XUDD)
Synonyms:
MDL No: MFCD10697413
Molecular Formula: C6H6BClO3
Molecular Weight: 172.3740

Identification/Properties

Properties
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
172.371g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
172.01g/mol
Monoisotopic Mass:
172.01g/mol
Topological Polar Surface Area:
60.7A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
133
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:
H302-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-Chloro-3-hydroxyphenyl)boronic acid, also known as 4-Chloro-3-hydroxybenzeneboronic acid, is a versatile organic compound widely used in chemical synthesis as a key building block. Its unique chemical structure and reactivity make it an essential reagent in various reactions and transformations.This compound plays a crucial role in the field of organic chemistry, particularly in Suzuki-Miyaura cross-coupling reactions. In this reaction, (4-Chloro-3-hydroxyphenyl)boronic acid acts as a boronic acid partner, participating in the formation of carbon-carbon bonds. This reaction is highly valuable in the synthesis of complex organic molecules and pharmaceuticals.Furthermore, (4-Chloro-3-hydroxyphenyl)boronic acid can be utilized in the preparation of arylboronic acid esters, which are important intermediates in organic synthesis. These esters can undergo various transformations to introduce functional groups or further modify the molecular structure.Overall, the application of (4-Chloro-3-hydroxyphenyl)boronic acid in chemical synthesis encompasses a wide range of reactions and processes, making it an indispensable tool for synthetic chemists in the creation of novel compounds and materials.