4-Iodophenylboronic Acid - CAS 5122-99-6
Catalog: |
BB027377 |
Product Name: |
4-Iodophenylboronic Acid |
CAS: |
5122-99-6 |
Synonyms: |
(4-iodophenyl)boronic acid; (4-iodophenyl)boronic acid |
IUPAC Name: | (4-iodophenyl)boronic acid |
Description: | Reagent used for: 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. |
Molecular Weight: | 247.83 |
Molecular Formula: | C6H6IO2B |
Canonical SMILES: | B(C1=CC=C(C=C1)I)(O)O |
InChI: | InChI=1S/C6H6BIO2/c8-6-3-1-5(2-4-6)7(9)10/h1-4,9-10H |
InChI Key: | PELJYVULHLKXFF-UHFFFAOYSA-N |
Boiling Point: | 333.1 °C at 760 mmHg |
Melting Point: | 326-330 °C (lit.) |
Flash Point: | Not applicable |
Purity: | ≥ 95.0 % |
Density: | 1.95 g/cm3 |
Appearance: | Solid |
MDL: | MFCD01319014 |
LogP: | -0.02900 |
GHS Hazard Statement: | H302 (97.83%): Harmful if swallowed [Warning Acute toxicity, oral] |
Precautionary Statement: | P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P340, P305+P351+P338, P312, P321, P330, P332+P313, P337+P313, P362, P403+P233, P405, and P501 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
CN-112687878-A | Electrochemical device and electronic device | 20201225 |
CN-112198309-A | Chemiluminescence substrate detection kit with high sensitivity and stable signal | 20200929 |
CN-111647011-A | Preparation method of monohalogenated phenylboronic acid | 20200716 |
CN-110850097-A | Calprotectin detection kit and detection method | 20191107 |
CN-110668960-A | Preparation method of alpha-aryl alpha-aminoketone compound | 20191022 |
PMID | Publication Date | Title | Journal |
23013456 | 20121005 | Direct amidation of carboxylic acids catalyzed by ortho-iodo arylboronic acids: catalyst optimization, scope, and preliminary mechanistic study supporting a peculiar halogen acceleration effect | The Journal of organic chemistry |
17297238 | 20070201 | Enhancing effect of phenylboronic acid compounds and their interactions with the diol groups of saccharides in a capillary electrophoresis-chemiluminescence detection system | Analytical sciences : the international journal of the Japan Society for Analytical Chemistry |
17141265 | 20070110 | A cost effective non-commercial ECL-solution for Western blot detections yielding strong signals and low background | Journal of immunological methods |
16716339 | 20060804 | Molecular recognition of mono- and disaccharides through interaction with p-iodophenylboronic acid in capillary electrophoresis with a chemiluminescence detection system | Journal of chromatography. A |
Complexity: | 102 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 247.95056 |
Formal Charge: | 0 |
Heavy Atom Count: | 10 |
Hydrogen Bond Acceptor Count: | 2 |
Hydrogen Bond Donor Count: | 2 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 247.95056 |
Rotatable Bond Count: | 1 |
Topological Polar Surface Area: | 40.5 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
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