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2,4,6-Trihydroxypyrimidine-5-carboxamide, also known as trihydroxypyrimidine-5-carboxamide, is a heterocyclic chemical compound with the molecular formula C5H4N4O4. It features a pyrimidine ring with three hydroxyl groups and a carboxamide group. 2,4,6-Trihydroxypyrimidine-5-carboxamide is a derivative of adenine and plays a significant role in various biological processes, such as DNA and RNA synthesis. It has been studied for its potential applications in pharmaceuticals, polymer materials, and for its antioxidant properties, including the scavenging of free radicals in the body.

56032-78-1

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56032-78-1 Usage

Uses

Used in Pharmaceutical Industry:
2,4,6-Trihydroxypyrimidine-5-carboxamide is used as a pharmaceutical compound for its potential role in the development of new drugs. Its involvement in DNA and RNA synthesis makes it a promising candidate for therapeutic applications.
Used in Polymer Material Development:
In the polymer industry, 2,4,6-Trihydroxypyrimidine-5-carboxamide is used as a building block for the creation of new polymer materials. Its unique structure and properties can contribute to the development of advanced materials with specific characteristics.
Used in Antioxidant Formulations:
2,4,6-Trihydroxypyrimidine-5-carboxamide is used as an antioxidant in various formulations. Its potential antioxidant properties and ability to scavenge free radicals make it a valuable component in health supplements and other products aimed at promoting overall health and well-being.

Check Digit Verification of cas no

The CAS Registry Mumber 56032-78-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,0,3 and 2 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 56032-78:
(7*5)+(6*6)+(5*0)+(4*3)+(3*2)+(2*7)+(1*8)=111
111 % 10 = 1
So 56032-78-1 is a valid CAS Registry Number.
InChI:InChI=1/C5H5N3O4/c6-2(9)1-3(10)7-5(12)8-4(1)11/h(H2,6,9)(H3,7,8,10,11,12)

56032-78-1SDS

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 6-hydroxy-2,4-dioxo-1H-pyrimidine-5-carboxamide

1.2 Other means of identification

Product number -
Other names 2,4,6-trioxo-hexahydro-pyrimidine-5-carboxylic acid amide

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:56032-78-1 SDS

56032-78-1Downstream Products

56032-78-1Relevant academic research and scientific papers

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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