1245563-08-9
5-Bromo-N-(2,2,2-trifluoroethyl)pyrimidin-2-amine
CAS: 1245563-08-9
Molecular Formula: C6H5BrF3N3
1245563-08-9 - Names and Identifiers
1245563-08-9 - Physico-chemical Properties
| Molecular Formula | C6H5BrF3N3 |
| Molar Mass | 256.02 |
| Storage Condition | Room temperature. |
| Sensitive | IRRITANT |
| MDL | MFCD17015846 |
1245563-08-9 - Introduction
5-Bromo-N-(2,2,2-trifluoroethyl)pyrimidin-2-amine (5-bromo-N-(2,2,2-trifluoroethyl)pyrimidin-2-amine) is an organic compound. The following is a description of its nature, use, preparation and safety information:
Nature:
-Appearance: It is a white solid.
-Molecular formula: C6H5BrF3N4.
-Molecular weight: 270.03g/mol.
-Melting point: about 152-155°C.
Use:
5-Bromo-N-(2,2,2-trifluoroethyl)pyrimidin-2-amine is an intermediate compound commonly used in drug development and organic synthesis.
Preparation Method:
5-Bromo-N-(2,2,2-trifluoroethyl)pyrimidin-2-amine can be obtained by the following synthetic route:
1. First, pyrimidin-2-amine is reacted with trifluoroethanol to obtain N-(2,2, 2-trifluoroethyl) pyrimidin-2-amine.
2. Then, N-(2,2,2-trifluoroethyl)pyrimidin-2-amine is reacted with bromine to obtain the final product 5-Bromo-N-(2,2,2-trifluoroethyl)pyrimidin-2-amine.
Safety Information:
All safety information regarding this compound has not been reported in detail. However, as an organic compound, it may have irritating or toxic effects on the human body. Appropriate laboratory safety and personal protective measures should be observed during use or handling. For detailed safety information, refer to the relevant chemical literature or the safety data sheet provided by the supplier.
Nature:
-Appearance: It is a white solid.
-Molecular formula: C6H5BrF3N4.
-Molecular weight: 270.03g/mol.
-Melting point: about 152-155°C.
Use:
5-Bromo-N-(2,2,2-trifluoroethyl)pyrimidin-2-amine is an intermediate compound commonly used in drug development and organic synthesis.
Preparation Method:
5-Bromo-N-(2,2,2-trifluoroethyl)pyrimidin-2-amine can be obtained by the following synthetic route:
1. First, pyrimidin-2-amine is reacted with trifluoroethanol to obtain N-(2,2, 2-trifluoroethyl) pyrimidin-2-amine.
2. Then, N-(2,2,2-trifluoroethyl)pyrimidin-2-amine is reacted with bromine to obtain the final product 5-Bromo-N-(2,2,2-trifluoroethyl)pyrimidin-2-amine.
Safety Information:
All safety information regarding this compound has not been reported in detail. However, as an organic compound, it may have irritating or toxic effects on the human body. Appropriate laboratory safety and personal protective measures should be observed during use or handling. For detailed safety information, refer to the relevant chemical literature or the safety data sheet provided by the supplier.
Last Update：2024-04-09 21:54:55
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1245563-08-9
4-Pyrimidinamine, 5-[(1,1-dimethylethyl)sulfonyl]-2-(4-pyridinyl)-
(-)-N-[(R)-sec-Butyl]-3,5-dinitrobenzamide
7-[(5-chloro-2,6-difluoro-4-pyrimidinyl)amino]-4-hydroxy-3-[(4-methoxy-2-sulphophenyl)azo]naphthalene-2-sulphonic acid, sodium salt
Einecs 267-360-0
2-(1,3-DIOXO-1,3-DIHYDRO-ISOINDOL-2-YL)-4-METHYLSULFANYL-BUTYRIC ACID METHYL ESTER
METHYL 4-[(3-CHLOROBENZYL)OXY]BENZENECARBOXYLATE
4-Pyrimidinamine, 5-[(1,1-dimethylethyl)sulfonyl]-2-(4-pyridinyl)-
(-)-N-[(R)-sec-Butyl]-3,5-dinitrobenzamide
7-[(5-chloro-2,6-difluoro-4-pyrimidinyl)amino]-4-hydroxy-3-[(4-methoxy-2-sulphophenyl)azo]naphthalene-2-sulphonic acid, sodium salt
Einecs 267-360-0
2-(1,3-DIOXO-1,3-DIHYDRO-ISOINDOL-2-YL)-4-METHYLSULFANYL-BUTYRIC ACID METHYL ESTER
METHYL 4-[(3-CHLOROBENZYL)OXY]BENZENECARBOXYLATE