Carbamic acid, (4-iodophenyl)methyl-, 1,1-dimethylethyl ester
Carbamic acid, (4-iodophenyl)methyl-, 1,1-dimethylethyl ester
CAS: 306768-12-7
Molecular Formula: C12H16INO2
Carbamic acid, (4-iodophenyl)methyl-, 1,1-dimethylethyl ester - Names and Identifiers
Carbamic acid, (4-iodophenyl)methyl-, 1,1-dimethylethyl ester - Physico-chemical Properties
| Molecular Formula | C12H16INO2 |
| Molar Mass | 333.17 |
Carbamic acid, (4-iodophenyl)methyl-, 1,1-dimethylethyl ester - Introduction
Carbamic acid, (4-iodophenyl)methyl-, 1,1-dimethylethyl ester, chemical formula C14H18INO2, is an organic compound. The following is a description of its nature, use, formulation and safety information:
Nature:
-Appearance: White crystalline solid
-Molecular weight: 363.21g/mol
-Melting point: 48-52 ° C
-Boiling point: 427.6 ° C
-Solubility: It has good solubility in some organic solvents, such as dimethylformamide and dichloromethane, and is insoluble in water.
Use:
Carbamic acid, (4-iodophenyl)methyl-, 1,1-dimethylethyl ester is a reagent commonly used in organic synthesis. Its main applications include:
-Substrate or reagent for nucleophilic substitution of benzene ring.
-The starting material for the synthesis of drugs or other organic compounds in the laboratory.
Method:
The preparation of Carbamic acid, (4-iodophenyl)methyl-, 1,1-dimethylethyl ester usually involves the following steps:
1. The first preparation of N-methyl aniline.
2. React N-methylaniline with Boc acid (tert-butoxycarbonyl) to form N-Boc-methylaniline.
3. Finally, N-Boc-methylaniline is reacted with iodide to obtain Carbamic acid, (4-iodophenyl)methyl-, 1,1-dimethylethyl ester.
Safety Information:
The safe operation of Carbamic acid, (4-iodophenyl)methyl-, 1,1-dimethylethyl ester shall follow the safety regulations of chemical laboratory. In general, you need to pay attention to the following:
-Avoid direct contact with skin and eyes, and wear personal protective equipment when using.
-The operation needs to be carried out in a well-ventilated laboratory to avoid inhaling its vapors.
-storage should be sealed in a dry, cool, ventilated place.
-Waste disposal to comply with local regulations.
Note: The information provided above is for reference only. Before using or handling this compound, be sure to consult relevant literature and safety information, and follow appropriate operating procedures and safety measures.
Nature:
-Appearance: White crystalline solid
-Molecular weight: 363.21g/mol
-Melting point: 48-52 ° C
-Boiling point: 427.6 ° C
-Solubility: It has good solubility in some organic solvents, such as dimethylformamide and dichloromethane, and is insoluble in water.
Use:
Carbamic acid, (4-iodophenyl)methyl-, 1,1-dimethylethyl ester is a reagent commonly used in organic synthesis. Its main applications include:
-Substrate or reagent for nucleophilic substitution of benzene ring.
-The starting material for the synthesis of drugs or other organic compounds in the laboratory.
Method:
The preparation of Carbamic acid, (4-iodophenyl)methyl-, 1,1-dimethylethyl ester usually involves the following steps:
1. The first preparation of N-methyl aniline.
2. React N-methylaniline with Boc acid (tert-butoxycarbonyl) to form N-Boc-methylaniline.
3. Finally, N-Boc-methylaniline is reacted with iodide to obtain Carbamic acid, (4-iodophenyl)methyl-, 1,1-dimethylethyl ester.
Safety Information:
The safe operation of Carbamic acid, (4-iodophenyl)methyl-, 1,1-dimethylethyl ester shall follow the safety regulations of chemical laboratory. In general, you need to pay attention to the following:
-Avoid direct contact with skin and eyes, and wear personal protective equipment when using.
-The operation needs to be carried out in a well-ventilated laboratory to avoid inhaling its vapors.
-storage should be sealed in a dry, cool, ventilated place.
-Waste disposal to comply with local regulations.
Note: The information provided above is for reference only. Before using or handling this compound, be sure to consult relevant literature and safety information, and follow appropriate operating procedures and safety measures.
Last Update：2024-04-09 21:00:56
