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2-Amino-5-pyrimidinecarboxyaldehyde

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CAS:120747-84-4
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CAS:120747-84-4
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CAS:120747-84-4
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CAS:120747-84-4
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CAS:120747-84-4
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2-Amino-5-pyrimidinecarboxyaldehyde Basic information
Product Name:2-Amino-5-pyrimidinecarboxyaldehyde
Synonyms:ASISCHEM C63547;2-AMINO-5-PYRIMIDINECARBOXYALDEHYDE;2-AMINO-PYRIMIDINE-5-CARBALDEHYDE;5-Pyrimidinecarboxaldehyde, 2-amino- (9CI);2-Amino-5-pyrimidinecarbaldehyde;2-Amino-pyrimidine-5-carbaldehyde ,97%;2-aminopyrimidine-5-carbaldehyde(SALTDATA: FREE);2-AMinopyriMidine-5-carboxaldehyde, 97%
CAS:120747-84-4
MF:C5H5N3O
MW:123.11
EINECS:
Product Categories:Heterocycle-Pyrimidine series;PYRIMIDINE;ALDEHYDE
Mol File:120747-84-4.mol
2-Amino-5-pyrimidinecarboxyaldehyde Structure
2-Amino-5-pyrimidinecarboxyaldehyde Chemical Properties
Melting point 209-214°C
Boiling point 372.7±34.0 °C(Predicted)
density 1.370±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
form solid
pka1.99±0.10(Predicted)
AppearanceOff-white to yellow Solid
InChIInChI=1S/C5H5N3O/c6-5-7-1-4(3-9)2-8-5/h1-3H,(H2,6,7,8)
InChIKeyDPOYRRAYGKTRAU-UHFFFAOYSA-N
SMILESC1(N)=NC=C(C=O)C=N1
CAS DataBase Reference120747-84-4(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 22-43-36/37/38
Safety Statements 36/37-37/39-26
WGK Germany 3
HazardClass IRRITANT
HS Code 29339900
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
Skin Sens. 1
MSDS Information
2-Amino-5-pyrimidinecarboxyaldehyde Usage And Synthesis
Chemical PropertiesLight brown solid
Synthesis Reference(s)Journal of Heterocyclic Chemistry, 28, p. 1281, 1991 DOI: 10.1002/jhet.5570280520
Synthesis
Ethyl 2-aminopyrimidine-5-carboxylate

308348-93-8

2-Amino-5-pyrimidinecarboxyaldehyde

120747-84-4

General procedure for the synthesis of 2-amino-5-pyrimidinecarboxaldehyde from methyl 2-aminopyrimidine-5-carboxylate: methyl 2-aminopyrimidine-5-carboxylate (300 mg, 2.0 mmol) was dissolved in methanol (5 mL) containing a few drops of water. Subsequently, lithium hydroxide (122 mg, 5.1 mmol) was added and the reaction mixture was stirred and reacted at 60 °C overnight. Upon completion of the reaction, the mixture was concentrated under reduced pressure, after which it was diluted with water and the pH was adjusted with 1 M HCl solution to 4. At this point, 2-aminopyrimidine-5-carboxylic acid precipitated as a white solid, which was isolated by vacuum filtration to give the product (244 mg, 90% yield). The structure of the product was confirmed by 1H NMR (DMSO-d6), δ: 12.73 (1H, broad peak), 8.63 (2H, single peak), 7.44 (2H, broad peak).

References[1] Patent: WO2012/62748, 2012, A1. Location in patent: Page/Page column 53-54
2-Amino-5-pyrimidinecarboxyaldehyde Preparation Products And Raw materials
Raw materialsEthanol-->Methanol-->Sulfuric acid-->Sodium-->N,N-Dimethylformamide-->Phosphorus oxitrichloride-->Chloroform-->Guanidine hydrochloride-->Bromoacetic acid-->Propanedial, 2-[(dimethylamino)methylene]-
Tag:2-Amino-5-pyrimidinecarboxyaldehyde(120747-84-4) Related Product Information
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