CAS 1193-22-2
:6-Amino-4(3H)-pyrimidinone
- 4(1H)-Pyrimidinone, 6-amino-
- 4(3H)-Pyrimidinone, 6-amino-
- 4-Amino-6-Hydroxy Pyrimidine
- 4-Amino-6-pyrimidinol
- 4-Hydroxy-6-aminopyrimidine
- 4-Oxy-6-aminopyrimidine
- 4-Pyrimidinol, 6-amino-
- 6-Amino-1H-pyrimidin-4-one
- 6-Amino-4(3H)-pyrimidinone
- 6-Aminopyrimidin-4(3H)-one
- 6-aminopyrimidin-4(1H)-one
- 6-hydroxypyrimidin-4(3H)-one
- See more synonyms
4-Amino-6-hydroxypyrimidine
CAS:Formula:C4H5N3OPurity:>98.0%(T)(qNMR)Color and Shape:White to Orange to Green powder to crystalMolecular weight:111.104(3H)-Pyrimidinone, 6-amino-
CAS:Formula:C4H5N3OPurity:98%Color and Shape:SolidMolecular weight:111.10204-Amino-6-hydroxypyrimidine
CAS:Controlled ProductApplications 4-Amino-6-hydroxypyrimidine (cas# 1193-22-2) is a compound useful in organic synthesis.
Formula:C4H5N3OColor and Shape:NeatMolecular weight:111.16-Aminopyrimidin-4-ol
CAS:6-Aminopyrimidin-4-ol is an intermediate in the synthesis of orotic acid. It is also a precursor to 6-chloropurine, which is used in the manufacture of orotic acid and 6-aminopurine. 6-Aminopyrimidin-4-ol can be prepared by benzannulation of phosphorus oxychloride with orotic acid or by hydrolysis of 6-chloropurine with thiourea. The latter method is preferred because it results in less waste.
6-Aminopyrimidin-4-ol is labile and must be stored under an inert gas at low temperature to prevent decomposition. It undergoes inactivating reactions with strong oxidizing agents, such as chlorine dioxide, peracetic acid, hydrogen peroxide, and potassium permanganate.
It also reacts with nucleophiles such as ammonia or amines to form stable tautFormula:C4H5N3OPurity:Min. 95%Color and Shape:PowderMolecular weight:111.1 g/molRef: 3D-FA11362
Discontinued product





