2-(4-Methylpiperazin-1-yl)pyridine-4-carbonitrile
2-(4-Methylpiperazin-1-yl)isonicotinonitrile
CAS: 1016501-27-1
Molecular Formula: C11H14N4
2-(4-Methylpiperazin-1-yl)pyridine-4-carbonitrile - Names and Identifiers
2-(4-Methylpiperazin-1-yl)pyridine-4-carbonitrile - Physico-chemical Properties
| Molecular Formula | C11H14N4 |
| Molar Mass | 202.26 |
| Storage Condition | 2-8°C |
| Sensitive | IRRITANT |
| MDL | MFCD09932504 |
2-(4-Methylpiperazin-1-yl)pyridine-4-carbonitrile - Introduction
2-(4-Methylpiperazin-1-yl)isonicotinonitrile(2-(4-methylpiperazin-1-yl) isonicotinic acid nitrile) is an organic compound with the formula C12H16N4.
Nature:
-Appearance: White or off-white solid
-Melting point: about 140-143 degrees Celsius
-relative molecular mass: about 220.28
-Solubility: Can be dissolved in most organic solvents, such as ethanol and chloroform
Use:
2-(4-methylpiperazin-1-yl) isonicotinic acid nitrile is mainly used in the field of organic synthesis, as an important intermediate in the field of medicine. It can be used to introduce different functional groups through various reactions to synthesize biologically active compounds, such as drugs and pesticides.
Preparation Method:
The preparation of 2-(4-methylpiperazin-1-yl) isonicotinic acid nitrile can be carried out by the following steps:
1.4-(methyl)-3-piperazinenitrile was synthesized by reacting 4-methyl piperazine with isocyanate.
2.4-(methyl)-3-piperazinenitrile is reacted with acetonitrile and sodium cyanide to generate 2-(4-methylpiperazin-1-yl) isonicotinic acid nitrile.
Safety Information:
There is less safety information about 2-(4-methylpiperazin-1-yl) isonicotinic acid nitrile, but as a basic rule for chemical substances, the following safety measures should be observed:
-Avoid direct contact with skin and eyes to avoid irritation or damage.
-Appropriate personal protective equipment, such as lab gloves and eye protection, should be used during operation.
-Operate in a well-ventilated place to avoid inhaling dust or vapor.
-Local regulations and guidelines should be observed during storage and disposal.
Please note, however, that this information is for informational purposes only and does not represent an adequate safety assessment. When using or handling this compound, be sure to refer to the relevant safety information and technical guidelines.
Nature:
-Appearance: White or off-white solid
-Melting point: about 140-143 degrees Celsius
-relative molecular mass: about 220.28
-Solubility: Can be dissolved in most organic solvents, such as ethanol and chloroform
Use:
2-(4-methylpiperazin-1-yl) isonicotinic acid nitrile is mainly used in the field of organic synthesis, as an important intermediate in the field of medicine. It can be used to introduce different functional groups through various reactions to synthesize biologically active compounds, such as drugs and pesticides.
Preparation Method:
The preparation of 2-(4-methylpiperazin-1-yl) isonicotinic acid nitrile can be carried out by the following steps:
1.4-(methyl)-3-piperazinenitrile was synthesized by reacting 4-methyl piperazine with isocyanate.
2.4-(methyl)-3-piperazinenitrile is reacted with acetonitrile and sodium cyanide to generate 2-(4-methylpiperazin-1-yl) isonicotinic acid nitrile.
Safety Information:
There is less safety information about 2-(4-methylpiperazin-1-yl) isonicotinic acid nitrile, but as a basic rule for chemical substances, the following safety measures should be observed:
-Avoid direct contact with skin and eyes to avoid irritation or damage.
-Appropriate personal protective equipment, such as lab gloves and eye protection, should be used during operation.
-Operate in a well-ventilated place to avoid inhaling dust or vapor.
-Local regulations and guidelines should be observed during storage and disposal.
Please note, however, that this information is for informational purposes only and does not represent an adequate safety assessment. When using or handling this compound, be sure to refer to the relevant safety information and technical guidelines.
Last Update：2024-04-09 21:54:55
