ChemicalBook--->CAS DataBase List--->669066-89-1

669066-89-1

669066-89-1 Structure

669066-89-1 Structure
IdentificationBack Directory
[Name]

3-AMINO-5-BROMOPYRIDINE-2-CARBOXAMIDE
[CAS]

669066-89-1
[Synonyms]

3-AMINO-5-BROMOPYRIDINE-2-CARBOXAMIDE
3-Amino-5-bromopyridine-3-carboxamide
2-Pyridinecarboxamide, 3-amino-5-bromo-
3-AMINO-5-BROMOPYRIDINE-2-CARBOXAMIDE ISO 9001:2015 REACH
[EINECS(EC#)]

200-589-5
[Molecular Formula]

C6H6BrN3O
[MDL Number]

MFCD11110235
[MOL File]

669066-89-1.mol
[Molecular Weight]

216.04
Chemical PropertiesBack Directory
[Boiling point ]

358.8±42.0 °C(Predicted)
[density ]

1.802±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[form ]

solid
[pka]

14.56±0.50(Predicted)
[Appearance]

Light yellow to brown Solid
[InChI]

InChI=1S/C6H6BrN3O/c7-3-1-4(8)5(6(9)11)10-2-3/h1-2H,8H2,(H2,9,11)
[InChIKey]

VKYMXWCCSJWUQY-UHFFFAOYSA-N
[SMILES]

C1(C(N)=O)=NC=C(Br)C=C1N
Safety DataBack Directory
[Symbol(GHS) ]

Skull and Crossbones (GHS06)
GHS06
[Signal word ]

Danger
[Hazard statements ]

H301-H317-H319
[Precautionary statements ]

P280-P301+P310-P305+P351+P338
[Hazard Codes ]

T
[Risk Statements ]

25-36-43
[Safety Statements ]

26-36/37-45
[RIDADR ]

UN 2811 6.1 / PGIII
[WGK Germany ]

WGK 3
[HazardClass ]

IRRITANT
[Storage Class]

6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
[Hazard Classifications]

Acute Tox. 3 Oral
Eye Irrit. 2
Skin Sens. 1
Spectrum DetailBack Directory
[Spectrum Detail]

3-AMINO-5-BROMOPYRIDINE-2-CARBOXAMIDE(669066-89-1)1HNMR
Hazard InformationBack Directory
[Synthesis]

5-BroMo-3-nitropyridine-2-carboxaMide

412035-35-9

3-AMINO-5-BROMOPYRIDINE-2-CARBOXAMIDE

669066-89-1

(4) Preparation of 3-amino-5-bromopyridine-2-carboxamide: 5-bromo-3-nitropyridine-2-carboxamide (400 mg, 1.63 mmol), ammonium chloride (435 mg, 8.15 mmol), and iron powder (273 mg, 4.89 mmol) were suspended in a solvent mixture of methanol (6 mL) and water (3 mL), and the reaction was stirred at 100°C for for 20 hours. After completion of the reaction, it was cooled to room temperature, filtered through diatomaceous earth and the diatomaceous earth was washed with methanol. The filtrates were combined and concentrated under reduced pressure. The residue was dissolved in chloroform and the organic layer was washed with water. The organic layer was separated and concentrated under reduced pressure to afford the target compound 3-amino-5-bromopyridine-2-carboxamide (246 mg, 70% yield).

[References]

[1] Patent: EP1757594, 2007, A1. Location in patent: Page/Page column 77
[2] Journal of the Chemical Society, 1952, p. 2042,2044
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