2-Amino-3-hydroxypyridine

2-Amino-3-hydroxypyridine Basic information
Product Name:2-Amino-3-hydroxypyridine
Synonyms:2-Amino-3-hydroxypyridine Vetec(TM) reagent grade, 98%;2-AMINO-3-HYDROXYPYRIDINE;2-AMINO-3-PYRIDINOL;2-AMINO-3-PYRIDOL;2-AMINO-PYRIDIN-3-OL;2-amino-3-pyridi;3-HYDROXY-2-AMINOPYRIDINE;3-PYRIDINOL, 2-AMINO-
CAS:16867-03-1
MF:C5H6N2O
MW:110.11
EINECS:240-886-8
Product Categories:Building Blocks;C5;Amines;Aromatics;Chemical Synthesis;Heterocyclic Building Blocks;Pyridines, Pyrimidines, Purines and Pteredines;pharmacetical;Pyridine;Pyridines derivates;Chemical Amines;Pyridines
Mol File:16867-03-1.mol
2-Amino-3-hydroxypyridine Structure
2-Amino-3-hydroxypyridine Chemical Properties
Melting point 168-172 °C (lit.)
Boiling point 206.4°C (rough estimate)
density 1.2111 (rough estimate)
vapor pressure 0.007-0.28Pa at 20-50℃
refractive index 1.4800 (estimate)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility DMSO (Slightly), Methanol (Slightly)
pka5.15±0.10(Predicted)
form Crystalline Powder
color Grayish-beige to brownish
BRN 109868
InChIKeyBMTSZVZQNMNPCT-UHFFFAOYSA-N
LogP-0.25 at 23℃ and pH7.02-7.04
Surface tension72.6mN/m at 1.053g/L and 20℃
CAS DataBase Reference16867-03-1(CAS DataBase Reference)
NIST Chemistry Reference2-Amino-3-hydroxypyridine(16867-03-1)
Safety Information
Hazard Codes Xi,T,Xn
Risk Statements 36/37/38-25-40
Safety Statements 26-45-37/39-28A-36-22
RIDADR UN2811
WGK Germany 3
Hazard Note Irritant
HazardClass 6.1
PackingGroup III
HS Code 29333999
MSDS Information
ProviderLanguage
2-Amino-3-pyridinol English
SigmaAldrich English
ACROS English
ALFA English
2-Amino-3-hydroxypyridine Usage And Synthesis
Chemical Propertieswhite to light yellow crystal powder
Uses2-Amino-3-hydroxypyridine was used as reagent in reaction of dimethyl acetylenedicarboxylate and triphenylphosphine to yield functionalized coumarins and 1,4-oxazines.
Synthesis Reference(s)Journal of Heterocyclic Chemistry, 14, p. 203, 1977 DOI: 10.1002/jhet.5570140206
General Description2-Amino-3-hydroxypyridine forms complexes with number of transition metals. It inhibits the corrosion of aluminium and copper in acidic solutions. It undergoes condensation with 2-hydroxy-1-naphthaldehyde and 2-hydroxybenzaldehyde to form Schiffs bases. It is useful in the preparation of clinical anti-inflammatory analgesics.
2,3-Dihydropyrido[2,3-d][1,3]oxazol-2-one 2H-Pyrido[3,2-b][1,4]oxazin-3(4H)-one 2-Amino-3-hydroxypyridine 3-ETHOXY-2-NITROPYRIDINE 2-(Acetylamino)-3-pyridyl acetate 7-CHLORO-2H-PYRIDO[3,2-B]-1,4-OXAZIN-3(4H)ONE 2-Amino-3-benzyloxypyridine 2-Nitro-3-hydroxypyridine 2-(2,5-DIMETHYL-1H-PYRROL-1-YL)PYRIDIN-3-OL 3-HYDROXY-6-METHYL-2-NITROPYRIDINE 3-[(3,4-DICHLOROBENZYL)OXY]PYRIDIN-2-AMINE 6-METHYL-2-NITRO-3-PYRIDYL 5-CHLORO-1,3-DIMETHYL-1H-PYRAZOLE-4-SULFONATE 2-Aminopyridine Tris(hydroxymethyl)aminomethane AMINO ACIDS 3-[(3-methylphenyl)methoxy]pyridin-2-amine 3-BROMO-2,6-BISNITRO-5-METHOXYPYRIDINE 6-METHYL-2-NITRO-3-PYRIDYL 2-CHLORONICOTINATE

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