| Identification | Back Directory | [Name]
2-Pyridinamine, 6-chloro-5-methyl | [CAS]
442129-37-5 | [Synonyms]
EOS-61005
6-Chloro-5-methyl-2-pyridinamine
6-chloro-5-methylpyridin-2-amine
2-Pyridinamine, 6-chloro-5-methyl
6-Chloro-5-methyl-2-pyridineamino
6-AMino-2-chloro-3-Methylpyridine
6-chloro-5-methyl-2-pyridine amine
6-Chloro-5-Methyl-pyridin-2-ylaMine
2-Pyridinamine,6-chloro-5-methyl-(9CI)
6-Chloro-5-methylpyridin-2-amine(For export only) | [Molecular Formula]
C6H7ClN2 | [MDL Number]
MFCD13193513 | [MOL File]
442129-37-5.mol | [Molecular Weight]
142.59 |
| Chemical Properties | Back Directory | [Melting point ]
90-92 °C | [Boiling point ]
270.8±35.0 °C(Predicted) | [density ]
1.260±0.06 g/cm3(Predicted) | [storage temp. ]
Keep in dark place,Inert atmosphere,2-8°C | [pka]
3.00±0.37(Predicted) | [Appearance]
Light brown to off-white Solid | [InChI]
InChI=1S/C6H7ClN2/c1-4-2-3-5(8)9-6(4)7/h2-3H,1H3,(H2,8,9) | [InChIKey]
KPZRCZMNXPBHEH-UHFFFAOYSA-N | [SMILES]
C1(N)=NC(Cl)=C(C)C=C1 |
| Hazard Information | Back Directory | [Synthesis]
The general procedure for the synthesis of 6-chloro-5-methyl-2-pyridinamine from the compound (CAS:936727-56-9) was as follows: to a 50 mL reaction flask was added II-1 (2.26 g, 10 mmol), methanol (20 mL), and concentrated hydrochloric acid (1 equiv). The reaction mixture was heated to 70 °C and kept for 1 hour. Upon completion of the reaction, the mixture was concentrated, followed by the addition of 10 mL of water. The pH of the reaction system was adjusted to neutral with sodium hydroxide solution. Finally, the solid was collected by filtration to afford 1.2 g of the target product 6-chloro-5-methyl-2-pyridinamine in 85% yield. | [References]
[1] Patent: CN108658851, 2018, A. Location in patent: Paragraph 0061; 0062; 0063
[2] Patent: WO2008/141119, 2008, A2. Location in patent: Page/Page column 80-81 |
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Energy Chemical
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