6-tert-Butyl-2-hydroxy-pyrimidine-4-carboxylic acid - Names and Identifiers
6-tert-Butyl-2-hydroxy-pyrimidine-4-carboxylic acid - Physico-chemical Properties
Molecular Formula | C9H12N2O3
|
Molar Mass | 196.2 |
Storage Condition | Room Temprature |
Sensitive | Irritant |
MDL | MFCD11049200 |
6-tert-Butyl-2-hydroxy-pyrimidine-4-carboxylic acid - Risk and Safety
6-tert-Butyl-2-hydroxy-pyrimidine-4-carboxylic acid - Introduction
Pyrene (6-tert-butyl-2-hydroxypyrimidine-4-carboxylic acid) is an organic compound. Its chemical formula is C11H15N3O3 and its molecular weight is 237.26g/mol. The following is a detailed description of the properties, uses, preparation and safety information of the compound:
Nature:
-acid is a white solid.
-It is stable at room temperature, slightly soluble in water at room temperature, and soluble in organic solvents such as methanol, dimethyl sulfoxide, etc.
Use:
-acid has some applications in the pharmaceutical field, including as a drug intermediate.
-It can be used to synthesize biologically active compounds, such as antitumor drugs, antiviral drugs, etc.
Preparation Method:
The preparation of acid is generally achieved by chemical synthesis.
-The specific synthesis method may be as follows: firstly, 2-(tert-butylamino)-4-methylpyrimidine is synthesized from an appropriate starting material, and then further reacted under appropriate conditions to react methyl pyrimidine with sodium cyanate to obtain 2-cyano-4-methylpyrimidine. Finally, acid is obtained by hydrolysis reaction.
Safety Information:
-the safety of acid is high, but it is still necessary to pay attention to follow the safety operation procedures of chemical laboratories.
-Wear appropriate personal protective equipment, such as lab gloves, glasses, etc., to avoid direct contact with skin, eyes and mouth.
-When conducting experiments or operations, avoid toxic gases, vapors or dust, and keep the room well ventilated.
-When storing and handling the compound, avoid contact with strong oxidants and strong acids to prevent dangerous chemical reactions.
Last Update:2024-04-09 21:00:56