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5-FORMYLURACIL

5-FORMYLURACIL Basic information
Product Name:5-FORMYLURACIL
Synonyms:5-FORMILURACIL;5-FORMYLURACIL;2,4-dihydroxypyrimidine-5-carbaldehyde;1,2,3,4-TETRAHYDRO-2,4-DIOXOPYRIMIDINE-5-CARBALDEHYDE;AURORA KA-650;RARECHEM AH CK 0106;5-Pyrimidinecarboxaldehyde, 1,2,3,4-tetrahydro-2,4-dioxo- (6CI,7CI,8CI,9CI);5-Formyluracil 98%
CAS:1195-08-0
MF:C5H4N2O3
MW:140.1
EINECS:
Product Categories:Nucleotides and Nucleosides;5-FOA;Bases & Related Reagents;Nucleotides;Building Blocks;Heterocyclic Building Blocks;PYRIMIDINE;Pyridines, Pyrimidines, Purines and Pteredines;Heterocyclic Compounds;Pyrimidines
Mol File:1195-08-0.mol
5-FORMYLURACIL Structure
5-FORMYLURACIL Chemical Properties
Melting point >300 °C (dec.) (lit.)
density 1.567±0.06 g/cm3(Predicted)
storage temp. Inert atmosphere,Store in freezer, under -20°C
solubility DMSO (Slightly), Methanol (Slightly)
pka7.27±0.10(Predicted)
form Solid
color White to Pale Yellow
Sensitive Air Sensitive
InChIKeyOHAMXGZMZZWRCA-UHFFFAOYSA-N
CAS DataBase Reference1195-08-0(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
Hazard Note Irritant
HS Code 29349990
MSDS Information
ProviderLanguage
SigmaAldrich English
5-FORMYLURACIL Usage And Synthesis
Chemical PropertiesWhite Powder
UsesNucleoside derivatives of 5-substituted uracil have been explored for their potential application as anti-viral agents and in the treatment of tumors.
Uses5-Formyluracil may be used for the preparation of covalently linked base with 5-aminocytosine pair via Schiff base formation.
DefinitionChEBI: A pyrimidone resulting from the formal oxidation of the alcoholic hydroxy group of 5-hydroxymethyluracil to the corresponding aldehyde. It is a major one-electron photooxidation product of thymine in oligodeoxynucleotides.
Synthesis Reference(s)Tetrahedron Letters, 7, p. 5253, 1966 DOI: 10.1016/0005-2760(66)90119-6
5-FORMYLURACIL Preparation Products And Raw materials
Raw materials2,4-Dihydroxypyrimidine-5-carboxylic acid-->Thymine
Preparation Products5-Hydroxymethyluracil
5-ACETYL-1-(4-METHYLPIPERAZINO)-2,4(1H,3H)-PYRIMIDINEDIONE 5-ACETYL-3-(4-BROMOBENZYL)-1-(4-CHLOROPHENYL)-2,4(1H,3H)-PYRIMIDINEDIONE 5-CARBETHOXYURACIL ETHYL N-([1-(4-METHOXYPHENYL)-2,4-DIOXO-1,2,3,4-TETRAHYDRO-5-PYRIMIDINYL]CARBONYL)CARBAMATE 2-[5-([(ETHOXYCARBONYL)AMINO]CARBONYL)-2,4-DIOXO-3,4-DIHYDRO-1(2H)-PYRIMIDINYL]ETHYL 3-CHLOROBENZENECARBOXYLATE ETHYL N-[(1-MORPHOLINO-2,4-DIOXO-1,2,3,4-TETRAHYDRO-5-PYRIMIDINYL)CARBONYL]CARBAMATE 5-ACETYL-1-METHYL-1H-PYRIMIDINE-2,4-DIONE ETHYL N-([1-(2-HYDROXYETHYL)-2,4-DIOXO-1,2,3,4-TETRAHYDRO-5-PYRIMIDINYL]CARBONYL)CARBAMATE 5-ACETYL-1-[(4-CHLOROBENZYL)OXY]-2,4(1H,3H)-PYRIMIDINEDIONE 2,4-Dihydroxypyrimidine-5-carboxylic acid 5-ACETYL-1-PIPERIDINO-2,4(1H,3H)-PYRIMIDINEDIONE ETHYL N-[(1-METHOXY-2,4-DIOXO-1,2,3,4-TETRAHYDRO-5-PYRIMIDINYL)CARBONYL]CARBAMATE 6-AMINO-1,3-DIMETHYL-2,4-DIOXO-1,2,3,4-TETRAHYDROPYRIMIDINE-5-CARBALDEHYDE 5-ACETYL-1-(2-HYDROXY-ETHYL)-1H-PYRIMIDINE-2,4-DIONE 5-ACETYL-1-METHOXY-2,4(1H,3H)-PYRIMIDINEDIONE ETHYL N-((1-[(4-CHLOROBENZYL)OXY]-2,4-DIOXO-1,2,3,4-TETRAHYDRO-5-PYRIMIDINYL)CARBONYL)CARBAMATE 1,3-DIMETHYLURACIL-5-CARBOXALDEHYDE 5-ACETYL-1-(4-CHLOROPHENYL)-2,4(1H,3H)-PYRIMIDINEDIONE
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