Thiourea, N-2-pyrimidinyl-
1-(Pyrimidin-2-yl)thiourea
CAS: 31437-20-4
Molecular Formula: C5H6N4S
Thiourea, N-2-pyrimidinyl- - Names and Identifiers
Thiourea, N-2-pyrimidinyl- - Physico-chemical Properties
| Molecular Formula | C5H6N4S |
| Molar Mass | 154.19 |
| Density | 1.482±0.06 g/cm3(Predicted) |
| Melting Point | 278-280°C |
| Boling Point | 343.6±25.0 °C(Predicted) |
| pKa | 10.88±0.70(Predicted) |
| Sensitive | IRRITANT |
| MDL | MFCD02662218 |
Thiourea, N-2-pyrimidinyl- - Risk and Safety
| Risk Codes | R20/21/22 - Harmful by inhalation, in contact with skin and if swallowed. R36/37/38 - Irritating to eyes, respiratory system and skin. |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. |
Thiourea, N-2-pyrimidinyl- - Introduction
1-(Pyrimidin-2-yl)thiourea is an organic compound containing pyrimidine and thiourea groups in its structure. Its chemical formula is C5H6N4S.
1-(Pyrimidin-2-yl)thiourea mainly exists as a heterocyclic organic compound, which has certain biological activity and application value. Its use mainly includes the following aspects:
1. drug research: 1-(Pyrimidin-2-yl)thiourea and its derivatives are commonly used in drug research, as the starting point for the synthesis of new drug molecules or the basic structural unit of drug activity.
2. pesticide manufacturing: the compound can be used to synthesize some fungicides and herbicides and other pesticides.
3. Chemical reagents: 1-(Pyrimidin-2-yl)thiourea is also commonly used as a catalyst and intermediate in organic synthesis to generate other compounds.
The preparation method of
1-(Pyrimidin-2-yl)thiourea is relatively simple. It can be obtained by reacting a pyrimidine with thiourea under appropriate conditions. The specific synthesis method can be implemented in the chemical laboratory, which requires a certain basis of organic synthesis and experimental techniques.
Regarding the safety information of this compound, the following points need to be noted:
1. 1-(Pyrimidin-2-yl)thiourea may be irritating and sensitizing to the human body, so you should follow the safe operating procedures of the chemical laboratory and wear appropriate personal protective equipment.
2. The compound should be stored in a sealed container, avoid contact with oxygen, moisture and strong oxidants.
3. in the treatment and disposal of the need to pay attention to environmental protection, to avoid pollution to the environment.
1-(Pyrimidin-2-yl)thiourea mainly exists as a heterocyclic organic compound, which has certain biological activity and application value. Its use mainly includes the following aspects:
1. drug research: 1-(Pyrimidin-2-yl)thiourea and its derivatives are commonly used in drug research, as the starting point for the synthesis of new drug molecules or the basic structural unit of drug activity.
2. pesticide manufacturing: the compound can be used to synthesize some fungicides and herbicides and other pesticides.
3. Chemical reagents: 1-(Pyrimidin-2-yl)thiourea is also commonly used as a catalyst and intermediate in organic synthesis to generate other compounds.
The preparation method of
1-(Pyrimidin-2-yl)thiourea is relatively simple. It can be obtained by reacting a pyrimidine with thiourea under appropriate conditions. The specific synthesis method can be implemented in the chemical laboratory, which requires a certain basis of organic synthesis and experimental techniques.
Regarding the safety information of this compound, the following points need to be noted:
1. 1-(Pyrimidin-2-yl)thiourea may be irritating and sensitizing to the human body, so you should follow the safe operating procedures of the chemical laboratory and wear appropriate personal protective equipment.
2. The compound should be stored in a sealed container, avoid contact with oxygen, moisture and strong oxidants.
3. in the treatment and disposal of the need to pay attention to environmental protection, to avoid pollution to the environment.
Last Update：2024-04-10 22:40:09
