74025-90-4

Basic information

• Product Name: 2-amino-4-(3,6-dihydropyridin-1(2H)-yl)-6-[(methoxycarbonyl)amino]-1-oxo-1,6-dihydropyrimidin-1-ium
• CAS NO: 74025-90-4
• Molecular Formula: C₁₁H₁₆N₅O₃
• Molecular Weight: 266.2759
• Mol File: 74025-90-4.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 2-amino-4-(3,6-dihydropyridin-1(2H)-yl)-6-[(methoxycarbonyl)amino]-1-oxo-1,6-dihydropyrimidin-1-ium(CAS DataBase Reference)
• NIST Chemistry Reference: 2-amino-4-(3,6-dihydropyridin-1(2H)-yl)-6-[(methoxycarbonyl)amino]-1-oxo-1,6-dihydropyrimidin-1-ium(74025-90-4)
• EPA Substance Registry System: 2-amino-4-(3,6-dihydropyridin-1(2H)-yl)-6-[(methoxycarbonyl)amino]-1-oxo-1,6-dihydropyrimidin-1-ium(74025-90-4)

Safety Data

• Hazardous Substances Data: 74025-90-4(Hazardous Substances Data)

Usage

Properties

1. Chemical name: 2-amino-4-(3,6-dihydropyridin-1(2H)-yl)-6-[(methoxycarbonyl)amino]-1-oxo-1,6-dihydropyrimidin-1-ium
2. Molecular structure: Complex molecular structure containing an amino group, a dihydropyrimidin-1-ium moiety, and a methoxycarbonyl group
3. Potential pharmaceutical applications: Structure suggests potential biological activity
4. Usage: May be used in drug development, as a research tool, or in chemical synthesis
5. Need for further research: Further studies needed to fully understand properties and potential uses

Specific content

Amino group
Dihydropyrimidin-1-ium moiety
Methoxycarbonyl group
Complex molecular structure
Potential pharmaceutical applications
Usage in drug development, research, or chemical synthesis
Need for further research to fully understand properties and potential uses

Upstream product

• 694-05-3 1,2,3,6-tetrahydropyridine 
• 86134-94-3 2-amino-6-(methoxycarbonyl)amino-4-(p-tolylsulfonyl)oxypyrimidine 1-oxide 
• 79-22-1 methyl chloroformate 
• 68020-78-0 2,6-diamino-4-(1,2,3,6-tetrahydro-1-pyridyl)pyrimidine 1-oxide 
• 68020-76-8 4-(1,2,3,6-tetrahydro-1-pyridyl)-2,6-bis(methoxycarbonylamino)-pyrimidine 1-oxide 
• 86134-93-2 methyl 2-amino-6-(p-tolylsulfonyl)oxy-4-pyrimidinecarbamate 
• 86134-92-1 methyl 2-amino-1,6-dihydro-6-oxo-4-pyrimidinecarbamate 
• 68020-80-4 N-cyanoacetyl-1,2,3,6-tetrahydropyridine 
• 68020-77-9 methyl 5-<3,6-dihydro-1(2H)-pyridyl>-2-oxo-2H-<1,2,4>-oxadiazolo<2,3-a>pyrimidine-7-carbamate 

Downstream Products

• 83395-28-2 butyl 7-<3,6-dihydro-1(2H)-pyridyl>-2H-<1,2,4>oxadiazolo<2,3-a>pyrimidine-5-carbamate 
• 86553-26-6 i-butyl 7-<3,6-dihydro-1(2H)-pyridyl>-2H-<1,2,4>oxadiazolo<2,3-a>pyrimidine-5-carbamate 
• 83395-25-9 methyl 7-<3,6-dihydro-1(2H)-pyridyl>-2-oxo-2H-<1,2,4>-oxadiazolo<2,3-c>pyrimidine-5-carbamate 

Relevant articles and documents

Pyrimidinecarbamate derivatives as intermediates

2,4-Disubstituted 6-[3,6-dihydro-1(2H)-pyridyl]pyrimidine-3-oxides of the formula STR1 wherein R1 is lower alkyl or lower alkoxy-lower alkyl, R2 is hydrogen or --COOR3 wherein R3 is lower alkyl or lower alkoxy-l

61. Synthesis of 2-Oxo-2H-oxadiazolo-pyrimidine-5-carbamates

Thermal cyclization of the pyrimidine-N-oxide dicarbamate 2 gives a 95:5 mixture of the 2-oxo-2H-oxadiazolo- and pyrimidinecarbamates 3 and 4.An efficient procedure for the conversion of 3 to 4, and vice versa, is described.

Structure of new 2-oxo-2,8-dihydro-[1,2,4]oxadiazolo-[2,3-a]pyrimidine carbamates

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