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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)-

2-Iodophenylboronic acid

OB(c1ccccc1I)O Request for Quotation
Chemical Name: 2-Iodophenylboronic acid
CAS Number: 1008106-86-2
Product Number: AG0002XU(AGN-PC-04SWJJ)
Synonyms:
MDL No:
Molecular Formula: C6H6BIO2
Molecular Weight: 247.8261

Identification/Properties

Properties
MP:
189-194 °C
BP:
345.3 °C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
247.826g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
247.951g/mol
Monoisotopic Mass:
247.951g/mol
Topological Polar Surface Area:
40.5A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
110
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

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Chemical Structure


2-Iodophenylboronic acid is a versatile compound widely used in chemical synthesis as a valuable building block for various organic reactions. It serves as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and materials. Its unique properties make it a valuable reagent in Suzuki-Miyaura cross-coupling reactions, where it participates as a boronate ester to form carbon-carbon bonds. Additionally, 2-Iodophenylboronic acid is utilized in the construction of complex molecular architectures and heterocyclic compounds. Its application in organic synthesis showcases its significance in modern chemistry for creating novel compounds with diverse functionalities and applications.