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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-methylphenyl)-

OB(c1ccc(c(c1)C)Cl)O Request for Quotation
Chemical Name: Boronic acid, (4-chloro-3-methylphenyl)-
CAS Number: 161950-10-3
Product Number: AG001SJ7(AGN-PC-0L01XP)
Synonyms:
MDL No: MFCD02683104
Molecular Formula: C7H8BClO2
Molecular Weight: 170.4012

Identification/Properties

Properties
MP:
238-242 °C
BP:
317.5 °C at 760 mmHg
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
170.399g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
170.031g/mol
Monoisotopic Mass:
170.031g/mol
Topological Polar Surface Area:
40.5A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
132
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Chloro-3-methylphenylboronic acid, also known as $name$, holds a crucial role in chemical synthesis as a versatile building block for the creation of various organic compounds. With its unique chemical properties, this compound finds wide applications in the synthesis of pharmaceuticals, agrochemicals, and materials science.One significant application of 4-Chloro-3-methylphenylboronic acid is in Suzuki-Miyaura cross-coupling reactions. This powerful synthetic tool enables the formation of carbon-carbon bonds under mild reaction conditions, making it ideal for the construction of complex molecular structures. By using 4-Chloro-3-methylphenylboronic acid as a key starting material, chemists can efficiently synthesize biologically active molecules, such as pharmaceutical intermediates and natural products.Furthermore, this compound can participate in transition metal-catalyzed reactions to introduce the 4-chloro-3-methylphenyl group into target molecules, allowing for precise modifications and functionalizations. Its boronic acid functionality also facilitates further derivatization through various chemical transformations, expanding its utility in designing new compounds with tailored properties.In summary, 4-Chloro-3-methylphenylboronic acid serves as a valuable reagent in chemical synthesis, offering synthetic chemists a strategic tool for the construction of diverse organic molecules with applications across different industries.