Identification | More | [Name]
3-Amino-6-bromopyridine | [CAS]
13534-97-9 | [Synonyms]
2-AMINO-5-BROMOPYRIDINE 2-BROMO-5-AMINOPYRIDINE 3-AMINO-6-BROMOPYRIDINE 5-AMINO-2-BROMOPYRIDINE 5-BROMO-2-AMINOPYRIDINE 5-BROMOPYRIDIN-2-AMINE 5-BROMO-PYRIDIN-2-YLAMINE 6-BROMO-3-PYRIDINAMINE 6-BROMO-PYRIDIN-3-YLAMINE AKOS BBS-00004444 LABOTEST-BB LT00129606 TIMTEC-BB SBB003823 TIMTEC-BB SBB005540 2-Bromo-5-aminoyridine 6-BROMOPYRIDIN-3-AMINE 6-Bromo-[3]pyridylamine 2-Bromo-5 5-Amino-2-bromopyridine 96% | [EINECS(EC#)]
214-019-9 | [Molecular Formula]
C5H5BrN2 | [MDL Number]
MFCD00006323 | [Molecular Weight]
173.01 | [MOL File]
13534-97-9.mol |
Chemical Properties | Back Directory | [Appearance]
Light yellow needles | [Melting point ]
75 °C | [Boiling point ]
180 °C | [density ]
1.6065 (rough estimate) | [refractive index ]
1.5182 (estimate) | [storage temp. ]
Keep in dark place,Sealed in dry,Room Temperature | [form ]
Powder | [pka]
1.87±0.10(Predicted) | [color ]
Beige to brown-black | [Detection Methods]
GC | [BRN ]
109102 | [CAS DataBase Reference]
13534-97-9(CAS DataBase Reference) | [Storage Precautions]
Store under nitrogen |
Safety Data | Back Directory | [Hazard Codes ]
Xn,Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . S36:Wear suitable protective clothing . S37/39:Wear suitable gloves and eye/face protection . | [RIDADR ]
UN 2811 6.1/PG 3
| [WGK Germany ]
3
| [F ]
10 | [Hazard Note ]
Irritant | [HazardClass ]
IRRITANT | [PackingGroup ]
III | [HS Code ]
29333990 |
Hazard Information | Back Directory | [Chemical Properties]
Light yellow needles | [Uses]
3-Amino-6-bromopyridine may undergo polymerization via Buchwald–Hartwig amination in the presence of sodium tert-butoxide and XPhos(2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl) ligand yielding para-linked and meta-linked polyaminopyridines. | [General Description]
3-Amino-6-bromopyridine can be synthesized via bromination of 3-aminopyridine using N-bromosuccinimide in acetonitrile. |
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