81720-18-5
Methyl 2-(4-iodophenoxy)acetate
CAS: 81720-18-5
Molecular Formula: C9H9IO3
81720-18-5 - Names and Identifiers
| Name | Methyl 2-(4-iodophenoxy)acetate |
| Synonyms | Methyl 2-(4-iodophenoxy)acetate methyl 2-(4-iodophenoxy)acetate |
| CAS | 81720-18-5 |
81720-18-5 - Physico-chemical Properties
| Molecular Formula | C9H9IO3 |
| Molar Mass | 292.07 |
| Storage Condition | Room Temprature |
| Sensitive | Irritant |
| MDL | MFCD07113288 |
81720-18-5 - Introduction
Methyl 2-(4-iodophenoxy)acetate is an organic compound with the chemical formula C10H11IO3. It is a white solid, soluble in organic solvents such as ethanol and methylene chloride.
Methyl 2-(4-iodophenoxy)acetate is often used as an important intermediate in organic synthesis. It can be used to synthesize organic compounds with biological activity, such as drugs and pesticides. Such compounds are useful in the fields of blood clot inhibitors, anticancer drugs, and herbicides.
A common method for preparing Methyl 2-(4-iodophenoxy)acetate is through a nucleophilic aryl substitution reaction on the benzene ring. The methanol hydroxyl group on the benzene ring is first protected as an ester group, and then the aryl substitution reaction is carried out under alkaline conditions by using an alkaline reagent and an iodinated reagent. Finally, the target product is produced by a deprotection reaction under acidic conditions.
Regarding safety information, Methyl 2-(4-iodophenoxy)acetate is an organic compound and needs to follow relevant safe operating procedures in the laboratory. It can be irritating and toxic, so care should be taken to use protective gloves, goggles, and laboratory ventilation. In addition, this compound should be stored in a cool, dry place away from open flames and heat sources, and stored separately from oxidants and strong acids. In industrial and laboratory use, the relevant regulations and guidelines should be followed.
Methyl 2-(4-iodophenoxy)acetate is often used as an important intermediate in organic synthesis. It can be used to synthesize organic compounds with biological activity, such as drugs and pesticides. Such compounds are useful in the fields of blood clot inhibitors, anticancer drugs, and herbicides.
A common method for preparing Methyl 2-(4-iodophenoxy)acetate is through a nucleophilic aryl substitution reaction on the benzene ring. The methanol hydroxyl group on the benzene ring is first protected as an ester group, and then the aryl substitution reaction is carried out under alkaline conditions by using an alkaline reagent and an iodinated reagent. Finally, the target product is produced by a deprotection reaction under acidic conditions.
Regarding safety information, Methyl 2-(4-iodophenoxy)acetate is an organic compound and needs to follow relevant safe operating procedures in the laboratory. It can be irritating and toxic, so care should be taken to use protective gloves, goggles, and laboratory ventilation. In addition, this compound should be stored in a cool, dry place away from open flames and heat sources, and stored separately from oxidants and strong acids. In industrial and laboratory use, the relevant regulations and guidelines should be followed.
Last Update：2024-04-09 21:00:56
