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2-aminopyrimidine-4,6-diol is a heterocyclic chemical compound with the molecular formula C4H5N3O2. It features a unique structure with two nitrogen atoms and two oxygen atoms, making it a promising candidate for pharmaceutical applications and organic synthesis. Its versatile properties, including antiviral, antibacterial, and antioxidant activities, have been extensively studied, highlighting its potential in treating various diseases and disorders.

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  • 4425-67-6 Structure
  • Basic information

    1. Product Name: 2-aminopyrimidine-4,6-diol
    2. Synonyms: 2-AMINO-4,6(1H,5H)-PYRIMIDINEDIONE;4,6(1H,5H)-Pyrimidinedione, 2-amino- (9CI);2,3-Dihydro-2-iminopyrimidine-4,6(1H,5H)-dione;2-Amino-1,4,5,6-tetrahydropyrimidine-4,6-dione;2-Imino-2,3-dihydropyrimidine-4,6(1H,5H)-dione;2-amino-1H-pyrimidine-4,6-dione;2-amino-1H-pyrimidine-4,6-quinone;2-azanyl-1H-pyrimidine-4,6-dione
    3. CAS NO:4425-67-6
    4. Molecular Formula: C4H5N3O2
    5. Molecular Weight: 127.1014
    6. EINECS: 224-603-5
    7. Product Categories: PYRIMIDINE
    8. Mol File: 4425-67-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.84g/cm3
    6. Refractive Index: 1.752
    7. Storage Temp.: 2-8°C(protect from light)
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-aminopyrimidine-4,6-diol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-aminopyrimidine-4,6-diol(4425-67-6)
    11. EPA Substance Registry System: 2-aminopyrimidine-4,6-diol(4425-67-6)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 4425-67-6(Hazardous Substances Data)

4425-67-6 Usage

Uses

Used in Pharmaceutical Industry:
2-aminopyrimidine-4,6-diol is used as an active pharmaceutical ingredient for its antiviral, antibacterial, and antioxidant properties. Its ability to inhibit the growth of viruses, bacteria, and oxidative stress makes it a valuable compound in the development of new drugs and therapies.
Used in Organic Synthesis:
2-aminopyrimidine-4,6-diol serves as a building block in organic synthesis, allowing chemists to create a wide range of compounds with diverse applications. Its unique structure and reactivity make it an essential component in the synthesis of complex organic molecules.
Used in Disease Treatment:
2-aminopyrimidine-4,6-diol is being investigated for its potential use in the treatment of various diseases and disorders. Its biological and pharmacological properties have shown promise in addressing health issues, making it a valuable compound in medicinal research.

Check Digit Verification of cas no

The CAS Registry Mumber 4425-67-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,2 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4425-67:
(6*4)+(5*4)+(4*2)+(3*5)+(2*6)+(1*7)=86
86 % 10 = 6
So 4425-67-6 is a valid CAS Registry Number.
InChI:InChI=1/C4H5N3O2/c5-4-6-2(8)1-3(9)7-4/h1H2,(H3,5,6,7,8,9)

4425-67-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-1H-pyrimidine-4,6-dione

1.2 Other means of identification

Product number -
Other names 2-amino-4,6-dioxypyridine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4425-67-6 SDS

4425-67-6Relevant articles and documents

Prebiotic Origin of Pre-RNA Building Blocks in a Urea “Warm Little Pond” Scenario

Menor Salván,Bouza, Marcos,Fialho, David M.,Burcar, Bradley T.,Fernández, Facundo M.,Hud, Nicholas V.

, p. 3504 - 3510 (2020/10/02)

Urea appears to be a key intermediate of important prebiotic synthetic pathways. Concentrated pools of urea likely existed on the surface of the early Earth, as urea is synthesized in significant quantities from hydrogen cyanide or cyanamide (widely accepted prebiotic molecules), it has extremely high water solubility, and it can concentrate to form eutectics from aqueous solutions. We propose a model for the origin of a variety of canonical and non-canonical nucleobases, including some known to form supramolecular assemblies that contain Watson-Crick-like base pairs.The dual nucleophilic-electrophilic character of urea makes it an ideal precursor for the formation of nitrogenous heterocycles. We propose a model for the origin of a variety of canonical and noncanonical nucleobases, including some known to form supramolecular assemblies that contain Watson-Crick-like base pairs. These reactions involve urea condensation with other prebiotic molecules (e. g., malonic acid) that could be driven by environmental cycles (e. g., freezing/thawing, drying/wetting). The resulting heterocycle assemblies are compatible with the formation of nucleosides and, possibly, the chemical evolution of molecular precursors to RNA. We show that urea eutectics at moderate temperature represent a robust prebiotic source of nitrogenous heterocycles. The simplicity of these pathways, and their independence from specific or rare geological events, support the idea of urea being of fundamental importance to the prebiotic chemistry that gave rise to life on Earth.

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