4-Iodophenylboronic
4-Iodophenylboronic acid
CAS: 5122-99-6
Molecular Formula: C6H6BIO2
4-Iodophenylboronic - Names and Identifiers
| Name | 4-Iodophenylboronic acid |
| Synonyms | 4-Iodophenylboronic RARECHEM AH PB 0035 P-IODOPHENYLBORONIC ACID 4-IODOPHENYLBORONIC ACID 4-Iodophenylboronic acid p-Iodophenylboromc Acid p-Iodobenzeneboronic acid 4-IODOBENZENEBORONIC ACID Benzeneboronic acid, p-iodo- |
| CAS | 5122-99-6 |
| InChI | InChI=1/C6H6BIO2/c8-6-3-1-5(2-4-6)7(9)10/h1-4,9-10H |
| InChIKey | PELJYVULHLKXFF-UHFFFAOYSA-N |
4-Iodophenylboronic - Physico-chemical Properties
| Molecular Formula | C6H6BIO2 |
| Molar Mass | 247.83 |
| Density | 1.95±0.1 g/cm3(Predicted) |
| Melting Point | 326-330 °C (lit.) |
| Boling Point | 333.1±44.0 °C(Predicted) |
| Flash Point | 155.3°C |
| Water Solubility | 25 g/L |
| Vapor Presure | 5.53E-05mmHg at 25°C |
| Appearance | White crystal |
| Color | Light beige |
| pKa | 8.29±0.10(Predicted) |
| Storage Condition | Keep in dark place,Sealed in dry,Room Temperature |
| Sensitive | Light Sensitive |
| Refractive Index | 1.649 |
| MDL | MFCD01319014 |
4-Iodophenylboronic - Risk and Safety
| Risk Codes | R22 - Harmful if swallowed R36/37/38 - Irritating to eyes, respiratory system and skin. |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing. S37/39 - Wear suitable gloves and eye/face protection |
| WGK Germany | 3 |
| HS Code | 29319090 |
| Hazard Class | IRRITANT |
4-Iodophenylboronic - Introduction
4-Iodophenylboronic acid is an organic compound with the chemical formula C6H6BClO2. The following is a description of the nature, use, preparation and safety information of 4-Iodophenylboronic acid:
Nature:
- 4-Iodophenylboronic acid is a solid with a white crystalline appearance.
-It is stable at room temperature, but may decompose at high temperatures.
-May deliquesce when exposed to air.
-It is slightly soluble in water and soluble in organic solvents such as ethanol and dimethyl sulfoxide.
Use:
- 4-Iodophenylboronic acid is commonly used as a reagent in organic synthesis.
-It is an important aryl boronic acid, which can be used for the boronic acid coupling reaction of olefins to synthesize compounds with C- C bonds.
-It can also be used for organometallic chemical reactions and cross-coupling reactions.
Preparation Method:
-The preparation of 4-Iodophenylboronic acid is generally obtained by reacting phenylboronic acid with an iodine compound.
-The reaction is usually carried out in a suitable solvent, such as dichloromethane or acetonitrile.
-The reaction requires a certain temperature and time, often at room temperature for several hours or under heating for 30 minutes to several hours.
Safety Information:
- 4-Iodophenylboronic acid is relatively safe for human body at room temperature, but laboratory safety operation procedures should still be observed.
-It may be irritating to the eyes and skin, and direct exposure should be avoided when in contact.
-Wear appropriate personal protective equipment such as gloves and goggles during operation.
-after the end of the operation, should be timely cleaning, avoid ingestion or inhalation.
It should be noted that the specific use and treatment of chemical substances should be determined according to their characteristics and required experimental conditions. The safety operation regulations shall be strictly observed in the experimental operation.
Nature:
- 4-Iodophenylboronic acid is a solid with a white crystalline appearance.
-It is stable at room temperature, but may decompose at high temperatures.
-May deliquesce when exposed to air.
-It is slightly soluble in water and soluble in organic solvents such as ethanol and dimethyl sulfoxide.
Use:
- 4-Iodophenylboronic acid is commonly used as a reagent in organic synthesis.
-It is an important aryl boronic acid, which can be used for the boronic acid coupling reaction of olefins to synthesize compounds with C- C bonds.
-It can also be used for organometallic chemical reactions and cross-coupling reactions.
Preparation Method:
-The preparation of 4-Iodophenylboronic acid is generally obtained by reacting phenylboronic acid with an iodine compound.
-The reaction is usually carried out in a suitable solvent, such as dichloromethane or acetonitrile.
-The reaction requires a certain temperature and time, often at room temperature for several hours or under heating for 30 minutes to several hours.
Safety Information:
- 4-Iodophenylboronic acid is relatively safe for human body at room temperature, but laboratory safety operation procedures should still be observed.
-It may be irritating to the eyes and skin, and direct exposure should be avoided when in contact.
-Wear appropriate personal protective equipment such as gloves and goggles during operation.
-after the end of the operation, should be timely cleaning, avoid ingestion or inhalation.
It should be noted that the specific use and treatment of chemical substances should be determined according to their characteristics and required experimental conditions. The safety operation regulations shall be strictly observed in the experimental operation.
Last Update：2024-04-10 22:29:15
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Product Name: 4-Iodophenylboronic Acid Visit Supplier Webpage Request for quotationCAS: 5122-99-6
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QQ: 3008007409
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