(Z)-3-iodoprop-2-enoic acid
(Z)-(3)-Iodoacrylic acid
CAS: 6214-35-3
Molecular Formula: C3H3IO2
(Z)-3-iodoprop-2-enoic acid - Names and Identifiers
| Name | (Z)-(3)-Iodoacrylic acid |
| Synonyms | CIS-3-IODOACRYLIC ACID (Z)-(3)-IODOACRYLIC ACID (Z)-(3)-Iodoacrylic acid (Z)-3-iodoprop-2-enoic acid (2Z)-3-iodoprop-2-enoic acid (2Z)-3-Iodo-2-propenoic acid 2-Propenoic acid, 3-iodo-, (2Z)- |
| CAS | 6214-35-3 |
| InChI | InChI=1/C3H3IO2/c4-2-1-3(5)6/h1-2H,(H,5,6)/b2-1- |
(Z)-3-iodoprop-2-enoic acid - Physico-chemical Properties
| Molecular Formula | C3H3IO2 |
| Molar Mass | 197.96 |
| Density | 2.325g/cm3 |
| Melting Point | 65 °C |
| Boling Point | 248.3°C at 760 mmHg |
| Flash Point | 104°C |
| Vapor Presure | 0.00783mmHg at 25°C |
| Storage Condition | 2-8°C |
| Refractive Index | 1.636 |
(Z)-3-iodoprop-2-enoic acid - Introduction
(Z)-(3)-Iodoacrylic acid is an organic compound with the chemical formula C3H3IO2. The following is an introduction to some of its properties, uses, formulation and safety information:
Nature:
1. Appearance: colorless or yellowish liquid.
2. odor: has a special smell.
3. Melting point: about 20-22°C.
4. Boiling point: about 122-124°C.
5. Solubility: Soluble in water, alcohol and ether.
Use:
1. chemical synthesis: as an important intermediate in organic synthesis, used in the synthesis of other organic compounds.
2. Medical field: Some studies have shown that (Z)-(3)-Iodoacrylic acid may have certain anti-cancer activity, so it may have application potential in drug research and development.
Preparation Method:
A commonly used preparation method is obtained by reacting iodoacetone with vinyl trimethyl ammonium salt under alkaline conditions. Specific steps are as follows:
1. Under alkaline conditions, iodoacetone is reacted with vinyl trimethyl ammonium salt to obtain (Z)-3-iodopropenone.
2. Hydrolysis of (Z)-3-iodopropenone using alkali to obtain (Z)-(3)-Iodoacrylic acid.
Safety Information:
1. need to pay attention to prevent its contact with the eyes and skin, such as contact, should immediately rinse with plenty of water.
2. inhalation or ingestion may be harmful to health, should avoid inhalation of its vapor or exposure to its dust.
3. Store away from heat sources and open flames, and keep the container airtight.
4. It is recommended to wear appropriate personal protective equipment during operation, such as gloves, glasses, etc.
Please note that the information provided above is for reference only, and the specific experimental operation and use should be carried out according to the actual situation and safety regulations.
Nature:
1. Appearance: colorless or yellowish liquid.
2. odor: has a special smell.
3. Melting point: about 20-22°C.
4. Boiling point: about 122-124°C.
5. Solubility: Soluble in water, alcohol and ether.
Use:
1. chemical synthesis: as an important intermediate in organic synthesis, used in the synthesis of other organic compounds.
2. Medical field: Some studies have shown that (Z)-(3)-Iodoacrylic acid may have certain anti-cancer activity, so it may have application potential in drug research and development.
Preparation Method:
A commonly used preparation method is obtained by reacting iodoacetone with vinyl trimethyl ammonium salt under alkaline conditions. Specific steps are as follows:
1. Under alkaline conditions, iodoacetone is reacted with vinyl trimethyl ammonium salt to obtain (Z)-3-iodopropenone.
2. Hydrolysis of (Z)-3-iodopropenone using alkali to obtain (Z)-(3)-Iodoacrylic acid.
Safety Information:
1. need to pay attention to prevent its contact with the eyes and skin, such as contact, should immediately rinse with plenty of water.
2. inhalation or ingestion may be harmful to health, should avoid inhalation of its vapor or exposure to its dust.
3. Store away from heat sources and open flames, and keep the container airtight.
4. It is recommended to wear appropriate personal protective equipment during operation, such as gloves, glasses, etc.
Please note that the information provided above is for reference only, and the specific experimental operation and use should be carried out according to the actual situation and safety regulations.
Last Update：2024-04-09 19:05:51
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CAS: 6214-35-3
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CAS: 6214-35-3
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Email: 3008007409@qq.com
Mobile: 18021002903
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