(4,6-Dichloro-pyrimidin-2-yl)-ethyl-amine
(4,6-Dichloro-pyrimidin-2-yl)-ethyl-amine
CAS: 10371-48-9
Molecular Formula: C6H7Cl2N3
(4,6-Dichloro-pyrimidin-2-yl)-ethyl-amine - Names and Identifiers
| Name | (4,6-Dichloro-pyrimidin-2-yl)-ethyl-amine |
| Synonyms | 4,6-dichloro-N-ethylpyriMidin-2-aMine (4,6-Dichloro-pyrimidin-2-yl)-ethyl-amine |
| CAS | 10371-48-9 |
(4,6-Dichloro-pyrimidin-2-yl)-ethyl-amine - Physico-chemical Properties
| Molecular Formula | C6H7Cl2N3 |
| Molar Mass | 192.05 |
| Storage Condition | Room Temprature |
| Sensitive | Irritant |
| MDL | MFCD07396639 |
(4,6-Dichloro-pyrimidin-2-yl)-ethyl-amine - Introduction
(4,)-ethyl-amine is an organic compound whose molecular formula is C7H9Cl2N3. The following is a description of its nature, use, preparation and safety information:
Nature:
(4,)-ethyl-amine is a colorless to pale yellow solid with a distinctive odor. It is insoluble in water at normal temperature, but soluble in organic solvents such as alcohols, ethers and ketones. It is a chlorine-containing compound, so it has a certain degree of corrosion.
Use:
(4,)-ethyl-amine is an important organic synthesis intermediates. It is commonly used in the synthesis of pesticides, pharmaceuticals and other organic compounds. Because its structure contains a pyrimidine ring, it is often used in the synthesis of pyrimidine compounds. In addition, it can also be used in fields such as polymers and surfactants.
Preparation Method:
(4,)-ethyl-amine can be obtained by the functionalization reaction of pyrimidine. Typically, 4,6-dichloropyrimidine is first reacted with hydrochloric acid or sulfuric acid to give an intermediate product, and then reacted with ethylamine to give the target product (4,7)-ethyl-amine.
Safety Information:
(4,)-ethyl-amine in use need to strictly comply with the chemical laboratory safety practices. Due to its corrosive nature, it should be rinsed in time when in contact with skin or eyes. During operation and storage, reaction with oxidants, acids and alkaline substances should be avoided. In addition, a ventilated environment should be maintained to avoid inhalation of its vapors. If inhaled or ingested, seek medical advice immediately.
Nature:
(4,)-ethyl-amine is a colorless to pale yellow solid with a distinctive odor. It is insoluble in water at normal temperature, but soluble in organic solvents such as alcohols, ethers and ketones. It is a chlorine-containing compound, so it has a certain degree of corrosion.
Use:
(4,)-ethyl-amine is an important organic synthesis intermediates. It is commonly used in the synthesis of pesticides, pharmaceuticals and other organic compounds. Because its structure contains a pyrimidine ring, it is often used in the synthesis of pyrimidine compounds. In addition, it can also be used in fields such as polymers and surfactants.
Preparation Method:
(4,)-ethyl-amine can be obtained by the functionalization reaction of pyrimidine. Typically, 4,6-dichloropyrimidine is first reacted with hydrochloric acid or sulfuric acid to give an intermediate product, and then reacted with ethylamine to give the target product (4,7)-ethyl-amine.
Safety Information:
(4,)-ethyl-amine in use need to strictly comply with the chemical laboratory safety practices. Due to its corrosive nature, it should be rinsed in time when in contact with skin or eyes. During operation and storage, reaction with oxidants, acids and alkaline substances should be avoided. In addition, a ventilated environment should be maintained to avoid inhalation of its vapors. If inhaled or ingested, seek medical advice immediately.
Last Update：2024-04-09 21:04:16
