| Identification | Back Directory | [Name]
5-Bromo-[1,2,4]triazolo[1,5-a]pyridin-2-ylamine | [CAS]
1010120-55-4 | [Synonyms]
2-AMino-5-broMo-[1,2,4]triazolo[1,5-a]pyridin
5-bromo-[1,2,4]triazolo[1,5-a]pyridin-2-amine
2-Amino-5-bromo-1,2,4-triazolo[1,5-a]pyridine
1,2,4]Triazolo[1,5-a]pyridin-2-amine, 5-bromo-
5-Bromo-[1,2,4]triazolo[1,5-a]pyridin-2-ylamine
5-bromo-[1,2,4]trithiazole[1,5-A]pyridin-2-amine
5-Bromo-[1,2,4] triazolo[1,5-a]pyridine-2-ylamine
5-Bromo-[1,2,4]triazolo[1,5-a]pyridin-2-ylamine manufacturers | [EINECS(EC#)]
1592732-453-0 | [Molecular Formula]
C6H5BrN4 | [MDL Number]
MFCD11655928 | [MOL File]
1010120-55-4.mol | [Molecular Weight]
213.035 |
| Chemical Properties | Back Directory | [density ]
2.09 | [storage temp. ]
Keep in dark place,Inert atmosphere,2-8°C | [form ]
solid | [pka]
3.99±0.30(Predicted) | [Appearance]
White to off-white Solid | [InChI]
InChI=1S/C6H5BrN4/c7-4-2-1-3-5-9-6(8)10-11(4)5/h1-3H,(H2,8,10) | [InChIKey]
TVGFHUIJNZRKFW-UHFFFAOYSA-N | [SMILES]
C12=NC(N)=NN1C(Br)=CC=C2 |
| Hazard Information | Back Directory | [Uses]
5-Bromo-[1,2,4]triazolo[1,5-a]pyridin-2-ylamine is an important organic reagent that can be used as an organic intermediate for the synthesis of many organic compounds, such as N- (5-bromo- [1,2,4] triazolo [1,5-a] pyridin-2-yl) cyclopropylacetamide.
| [Synthesis]
2-Amino-6-bromopyridine could be used to synthesize 5-Bromo-[1,2,4]triazolo[1,5-a]pyridin-2-ylamine.
![5-Bromo-[1,2,4]triazolo[1,5-a]pyridin-2-ylamine](/NewsImg/2023-10-31/6383436521043138765517717.jpg "5-Bromo-[1,2,4]triazolo[1,5-a]pyridin-2-ylamine") | [References]
[1] Bioorganic and Medicinal Chemistry Letters, 2013, vol. 23, # 17, p. 5014 - 5021
[2] Patent: WO2009/155565, 2009, A1. Location in patent: Page/Page column 92-93
[3] Patent: WO2012/970, 2012, A1. Location in patent: Page/Page column 30-31
[4] Journal of Medicinal Chemistry, 2017, vol. 60, # 13, p. 5663 - 5672
[5] Patent: WO2010/141796, 2010, A2. Location in patent: Page/Page column 182 |
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