69099-99-6

Basic information

• Product Name: 2(1H)-Pyrimidinone, 4-amino-5-nitro- (9CI)
• Synonyms: 2(1H)-Pyrimidinone, 4-amino-5-nitro- (9CI);2(1H)-Pyrimidinone, 6-amino-5-nitro-;5-Nitrocytosine;NSC 266148;6-amino-5-nitro-1H-pyrimidin-2-one;6-Amino-5-nitro-2(1H)-pyrimidine;4-amino-5-nitro-1,2-dihydropyrimidin-2-one
• CAS NO: 69099-99-6
• Molecular Formula: C₄H₄N₄O₃
• Molecular Weight: 156.09956
• Product Categories: PYRIMIDINE
• Mol File: 69099-99-6.mol
• Article Data: 4

Chemical Properties

• Melting Point: >360℃
• Boiling Point: 553.4 °C at 760 mmHg
• Flash Point: 288.5 °C
• Appearance: /
• Density: 2.02 g/cm³
• Vapor Pressure: 7.43E-13mmHg at 25°C
• Refractive Index: 1.798
• CAS DataBase Reference: 2(1H)-Pyrimidinone, 4-amino-5-nitro- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 2(1H)-Pyrimidinone, 4-amino-5-nitro- (9CI)(69099-99-6)
• EPA Substance Registry System: 2(1H)-Pyrimidinone, 4-amino-5-nitro- (9CI)(69099-99-6)

Safety Data

• Hazardous Substances Data: 69099-99-6(Hazardous Substances Data)

Usage

General Description

2(1H)-Pyrimidinone, 4-amino-5-nitro- (9CI) is a chemical compound with the molecular formula C4H3N3O3. It is a derivative of pyrimidinone and contains an amino group and a nitro group. 2(1H)-Pyrimidinone, 4-amino-5-nitro- (9CI) has potential pharmaceutical applications, particularly as an intermediate in the synthesis of various bioactive molecules and pharmaceuticals. It has been studied for its potential anti-inflammatory, antibacterial, and antitumor properties. Additionally, it has been investigated for its potential as a building block in the development of new drugs and therapeutic agents. Overall, 2(1H)-Pyrimidinone, 4-amino-5-nitro- (9CI) is an important compound with potential applications in pharmaceutical research and development.

InChI:InChI=1/C4H4N4O3/c5-3-2(8(10)11)1-6-4(9)7-3/h1H,(H3,5,6,7,9)

Upstream product

• 71-30-7 Cytosine 
• 99968-75-9 2-ethoxy-5-nitro-3H-pyrimidin-4-one 
• 54308-63-3 2-ethylsulfanyl-pyrimidin-4-ylamine 

Downstream Products

• 611-08-5 5-nitrobarbituric acid 
• 122336-54-3 2-(4-amino-5-nitro-2-oxopyrimidin-1(2H)-yl)-5((benzoyloxy)methyl)tetrahydrofuran-3,4-diyl dibenzoate 
• 23899-73-2 4,5-diamino-1,2-dihydropyrimidin-2-one 

Relevant articles and documents

Phenyl-imidazolo-cytidine analogues: Structure-photophysical activity relationship and ability to detect single dna mismatch

To expand the arsenal of fluorescent cytidine analogues for the detection of genetic material, we synthesized para-substituted phenyl-imidazolo-cytidine (PhImC) analogues 5a-g and established a relationship between their structure and fluoresce

Mapping the landscape of potentially primordial informational oligomers: Oligodipeptides tagged with 2,4-disubstituted 5-aminopyrimidines as recognition elements

(Chemical Equation Presented) Bit different: 2,4-Dioxo- and 2,4-diamino-5-aminopyrimidine nuclei attached to an oligodipeptide backbone display a disparity in their base-pairing strength which is opposite to that shown by corresponding triazines. This behavior points to a remarkable correlation between pairing strength and ΔpKa values of pairs of complementary bases.