Benzenehexacarboxylic acid, 1,3,5-tri-2-propenyl ester
1,3,5-triallyl trihydrogen benzenehexacarboxylate
CAS: 67952-51-6
Molecular Formula: C21H18O12
Benzenehexacarboxylic acid, 1,3,5-tri-2-propenyl ester - Names and Identifiers
Benzenehexacarboxylic acid, 1,3,5-tri-2-propenyl ester - Physico-chemical Properties
| Molecular Formula | C21H18O12 |
| Molar Mass | 462.37 |
Benzenehexacarboxylic acid, 1,3,5-tri-2-propenyl ester - Introduction
1,3,5-triallyl trihydrogen benzenehexacarboxylate is an organic compound with the following properties:
-Appearance: yellow or brown liquid state.
-Solubility: Soluble in organic solvents, such as ether and alcohol.
The main uses of this compound are as follows:
-Chemical reaction: As a catalyst or reaction intermediate, it can participate in a variety of organic synthesis reactions.
-Field applications: Commonly used in resins, polymers, coatings and fine chemical products to improve the strength, heat resistance and corrosion resistance of materials.
The method for preparing 1,3,5-triallyl trihydrogen benzenehexacarboxylate is generally as follows:
1. Benzoquinone reacts with acrolein to generate 7,9-divaleryl benzene.
2. React 7,9-divaleryl benzene with formic acid to form 1,3,5-triallyl trihydrogen benzenehexacarboxylate.
When using 1,3,5-triallyl trihydrogen benzenehexacarboxylate, you need to pay attention to the following safety information:
-Protective measures: Personal protective equipment such as protective gloves, protective glasses and protective clothing should be worn.
-Storage conditions: Store in a dark, dry and well-ventilated place, away from fire and oxidizing agents.
-Precautions: Avoid contact with skin and inhalation of its vapor during operation. If you accidentally touch, rinse with water immediately and seek medical help.
-Appearance: yellow or brown liquid state.
-Solubility: Soluble in organic solvents, such as ether and alcohol.
The main uses of this compound are as follows:
-Chemical reaction: As a catalyst or reaction intermediate, it can participate in a variety of organic synthesis reactions.
-Field applications: Commonly used in resins, polymers, coatings and fine chemical products to improve the strength, heat resistance and corrosion resistance of materials.
The method for preparing 1,3,5-triallyl trihydrogen benzenehexacarboxylate is generally as follows:
1. Benzoquinone reacts with acrolein to generate 7,9-divaleryl benzene.
2. React 7,9-divaleryl benzene with formic acid to form 1,3,5-triallyl trihydrogen benzenehexacarboxylate.
When using 1,3,5-triallyl trihydrogen benzenehexacarboxylate, you need to pay attention to the following safety information:
-Protective measures: Personal protective equipment such as protective gloves, protective glasses and protective clothing should be worn.
-Storage conditions: Store in a dark, dry and well-ventilated place, away from fire and oxidizing agents.
-Precautions: Avoid contact with skin and inhalation of its vapor during operation. If you accidentally touch, rinse with water immediately and seek medical help.
Last Update：2024-04-09 19:05:00
