4-ForMyl-2-MethylthiopyriMidine
2-Methylsulfanyl-Pyrimidine-4-Carbaldehyde
CAS: 1074-68-6
Molecular Formula: C6H6N2OS
4-ForMyl-2-MethylthiopyriMidine - Names and Identifiers
4-ForMyl-2-MethylthiopyriMidine - Physico-chemical Properties
| Molecular Formula | C6H6N2OS |
| Molar Mass | 154.19 |
| Density | 1.29±0.1 g/cm3(Predicted) |
| Melting Point | 68°C |
| Boling Point | 110-112 °C(Press: 0.001 Torr) |
| Flash Point | 136°C |
| Vapor Presure | 0.00107mmHg at 25°C |
| pKa | -0.87±0.23(Predicted) |
| Storage Condition | under inert gas (nitrogen or Argon) at 2-8°C |
| Refractive Index | 1.583 |
4-ForMyl-2-MethylthiopyriMidine - Risk and Safety
| Safety Description | 24/25 - Avoid contact with skin and eyes. |
4-ForMyl-2-MethylthiopyriMidine - Introduction
2-Methylsulfanyl-pyrimidine-4-carbaldehyde (also known as MTMM) is an organic compound. The following is a description of its nature, use, preparation and safety information:
Properties: 2-Methylsulfanyl-pyrimidine-4-formaldehyde is a colorless liquid with a special smell. It is soluble in water and many organic solvents at room temperature. This compound is corrosive to a certain extent.
Application: 2-methylsulfanyl-pyrimidine-4-formaldehyde is mainly used as chemical reagent and intermediate. It can be used as a starting material for the synthesis of other organic compounds, such as drugs, dyes and pesticides. In addition, it can also be used in organic synthesis reactions and catalyst preparation.
Preparation Method: 2-Methylsulfanyl-pyrimidine-4-carbaldehyde is usually prepared by the following two methods:
a. 2-methylthio-pyrimidine reacts with sodium hydroxide solution to generate the corresponding phenolate, which is then converted into 2-methylthio-pyrimidine -4-formaldehyde by acid treatment.
B. 2-methylsulfanyl-pyrimidine reacts with formaldehyde, and is converted into 2-methylsulfanyl-pyrimidine-4-formaldehyde by the action of a catalyst.
Safety Information: 2-Methylsulfanyl-pyrimidine-4-formaldehyde is corrosive to the skin, eyes and respiratory tract, and can cause adverse reactions such as burning pain, redness and irritation after contact. Wear appropriate personal protective equipment during handling and contact to avoid direct inhalation of gases or contact with skin. In case of accidental contact, please rinse immediately with plenty of water and seek medical treatment. During storage and transportation, relevant safety regulations must be observed to avoid reactions with oxidants, strong acids and other substances.
Properties: 2-Methylsulfanyl-pyrimidine-4-formaldehyde is a colorless liquid with a special smell. It is soluble in water and many organic solvents at room temperature. This compound is corrosive to a certain extent.
Application: 2-methylsulfanyl-pyrimidine-4-formaldehyde is mainly used as chemical reagent and intermediate. It can be used as a starting material for the synthesis of other organic compounds, such as drugs, dyes and pesticides. In addition, it can also be used in organic synthesis reactions and catalyst preparation.
Preparation Method: 2-Methylsulfanyl-pyrimidine-4-carbaldehyde is usually prepared by the following two methods:
a. 2-methylthio-pyrimidine reacts with sodium hydroxide solution to generate the corresponding phenolate, which is then converted into 2-methylthio-pyrimidine -4-formaldehyde by acid treatment.
B. 2-methylsulfanyl-pyrimidine reacts with formaldehyde, and is converted into 2-methylsulfanyl-pyrimidine-4-formaldehyde by the action of a catalyst.
Safety Information: 2-Methylsulfanyl-pyrimidine-4-formaldehyde is corrosive to the skin, eyes and respiratory tract, and can cause adverse reactions such as burning pain, redness and irritation after contact. Wear appropriate personal protective equipment during handling and contact to avoid direct inhalation of gases or contact with skin. In case of accidental contact, please rinse immediately with plenty of water and seek medical treatment. During storage and transportation, relevant safety regulations must be observed to avoid reactions with oxidants, strong acids and other substances.
Last Update：2024-04-09 20:52:54
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