471933
4-Iodophenylboronic acid
≥95.0%
Synonym(s):
B-(4-iodophenyl)-boronic acid, p-Iodophenylboronic acid, p-iodo-benzeneboronic acid
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All Photos(2)
About This Item
Linear Formula:
IC6H4B(OH)2
CAS Number:
Molecular Weight:
247.83
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
≥95.0%
mp
326-330 °C (lit.)
SMILES string
OB(O)c1ccc(I)cc1
InChI
1S/C6H6BIO2/c8-6-3-1-5(2-4-6)7(9)10/h1-4,9-10H
InChI key
PELJYVULHLKXFF-UHFFFAOYSA-N
Application
Reagent used for
Reagent used in Preparation of
- Copper-mediated ligandless aerobic fluoroalkylation
- Palladium-catalyzed aerobic oxidative cross-coupling reactions
- Recyclable magnetic-nanoparticle-supported palladium catalyst for the Suzuki coupling reactions
- Oxidative hydroxylation using a copper (Cu) catalyst
- Ligand-free palladium-catalyzed Suzuki-Miyaura cross-coupling
- Homocoupling using gold salts as a catalyst
- Ruthenium (Ru)-catalyzed cross-coupling
- CuI-catalyzed Suzuki coupling reactions
- Palladium-catalyzed domino Heck-Mizoroki/Suzuki-Miyaura reactions
- Manganese triacetate-mediated radical additions of arylboronic acids to alkenes
Reagent used in Preparation of
- Pleuromutilin derivatives for ribosomal binding and antibacterial activity via "Click Chemistry"
- Liquid crystalline polyacetylene derivatives
Other Notes
Contains varying amounts of anhydride
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Customers Also Viewed
Hong Li et al.
Chemical communications (Cambridge, England), 47(27), 7880-7882 (2011-06-11)
The first ruthenium-catalyzed cross-coupling of aldehydes with arylboronic acids is reported. Various aliphatic and aromatic aldehydes are transformed to the corresponding arylketones. A total of 31 examples with moderate to excellent yields are presented, together with the results of an
Arne Dickschat et al.
Organic letters, 12(18), 3972-3974 (2010-08-20)
Arylboronic acids are shown to be valuable precursors for aryl radicals upon treatment with manganese triacetate. Under these oxidative conditions the intermediately generated aryl radicals undergo addition to olefins to give the arylhydroxylation products A in the presence of dioxygen.
Homocoupling of arylboronic acids catalyzed by simple gold salts
Matsuda, T.; et al.
Tetrahedron, 52, 4779-4781 (2011)
Samir Yahiaoui et al.
The Journal of organic chemistry, 76(8), 2433-2438 (2011-03-23)
A palladium(II)-catalyzed Heck-Mizoroki/Suzuki-Miyaura domino reaction involving metal coordinating dimethylaminoethyl vinyl ethers and a number of electron-rich and electron-deficient arylboronic acids has been developed. Through variation of the temperature and the concentration of the p-benzoquinone (p-Bq) ligand/reoxidant, conditions for the robust
B M Kinsey et al.
Nuclear medicine and biology, 20(1), 13-22 (1993-01-01)
Three iodinated phenylboronic acids have been synthesized: 4-iodophenylboronic acid (2a), 3-(4-iodobenzenesulfonamido)phenylboronic acid (5a) and 3-(5-dimethylamino-6-iodo-1-naphthalenesulfonamido)phenylboronic acid (6a). The corresponding no-carrier-added 125I derivatives 2b, 5b and 6b have been prepared in good yield by selective displacement of the tributylstannyl group. Compound
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