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5-ETHYL-2-THIOURACIL

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CAS:34171-37-4
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CAS:34171-37-4
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Products Intro: Product Name:5-Ethyl-2-thioxo-2,3-dihydropyrimidin-4(1H)-one
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5-ETHYL-2-THIOURACIL manufacturers

  • 5-Ethyl-2-thiouracil
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  • $1.00 / 1Kg
  • 2024-08-11
  • CAS:34171-37-4
  • Min. Order: 1Kg
  • Purity: 98%
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  • 5-ETHYL-2-THIOURACIL
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  • $15.00 / 1KG
  • 2021-07-13
  • CAS:34171-37-4
  • Min. Order: 1KG
  • Purity: 99%+ HPLC
  • Supply Ability: Monthly supply of 1 ton
  • 5-ETHYL-2-THIOURACIL
  • 5-ETHYL-2-THIOURACIL pictures
  • $15.00 / 1KG
  • 2021-07-10
  • CAS:34171-37-4
  • Min. Order: 1KG
  • Purity: 99%+ HPLC
  • Supply Ability: Monthly supply of 1 ton
5-ETHYL-2-THIOURACIL Basic information
Product Name:5-ETHYL-2-THIOURACIL
Synonyms:5-ETHYL-2-THIOURACIL;5-Ethyl-2-thiouracil ,98%;5-ethyl-2-sulfanylidene-1,2,3,4-tetrahydropyriMidin-4-one;5-Ethyl-2-thioxo-2,3-dihydropyriMidin-4(1H)-one;4(1H)-Pyrimidinone, 5-ethyl-2,3-dihydro-2-thioxo-;5-ETHYL-2-THIOURACIL USP/EP/BP
CAS:34171-37-4
MF:C6H8N2OS
MW:156.21
EINECS:
Product Categories:
Mol File:34171-37-4.mol
5-ETHYL-2-THIOURACIL Structure
5-ETHYL-2-THIOURACIL Chemical Properties
Melting point 191-193℃
density 1.29±0.1 g/cm3(Predicted)
storage temp. 2-8°C
solubility DMSO (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
form Solid
pka7.69±0.25(Predicted)
color Pale Yellow to Pale Beige
Safety Information
WGK Germany 3
HS Code 29335990
MSDS Information
ProviderLanguage
SigmaAldrich English
5-ETHYL-2-THIOURACIL Usage And Synthesis
Chemical PropertiesOff-white solid
Uses5-Ethyl-2-thiouracil is a modified nucleobase and a versatile reactant used in the synthesis. It was used as a reactant in the inhibition of Hepatitis B virus (HBV) replication.
Synthesis
Ethyl butyrate

105-54-4

Carbamimidothioic acid

17356-08-0

Ethyl formate

109-94-4

5-ETHYL-2-THIOURACIL

34171-37-4

Step D75: Synthesis of 5-ethyl-2-thio-2,3-dihydro-4(1H)-pyrimidinone 1. To a suspension of potassium tert-butanolate (12.08 g, 108 mmol) in THF (40 mL) under nitrogen protection was slowly added dropwise a mixed solution of ethyl butyrate (5.69 mL, 43.0 mmol) and ethyl formate (6.93 mL, 86 mmol) in ether (40.0 mL). 2. The reaction mixture was stirred at room temperature for 3 hours. 3. Upon completion of the reaction, the solvent was removed under reduced pressure to give an oily residue. 4. The residue was dissolved in isopropanol (350 mL) and thiourea (6.55 g, 86 mmol) was added. 5. The mixture was heated to reflux and stirred overnight. 6. At the end of the reaction, the reaction solution was concentrated under vacuum to give a solid product. 7. The solid product was dissolved in water and the pH was adjusted to 4 with acetic acid (AcOH). 8. 8. The aqueous phase was extracted with dichloromethane (DCM) and the organic layers were combined. 9. The organic layer was dried with anhydrous sodium sulfate (Na2SO4), filtered and concentrated under reduced pressure to give 5-ethyl-2-thiouracil (5.5 g, 82% yield) as a pink solid.

References[1] Patent: WO2012/76435, 2012, A1. Location in patent: Page/Page column 49
5-ETHYL-2-THIOURACIL Preparation Products And Raw materials
Raw materialsEthyl butyrate-->Carbamimidothioic acid-->Ethyl formate-->Tetrahydrofuran-->Potassium tert-butoxide-->Diethyl ether
Preparation Products5-Ethyluracil
Tag:5-ETHYL-2-THIOURACIL(34171-37-4) Related Product Information
5-ETHYL-2-THIOURACIL 2-Thiouracil 5-PROPYL-2-THIOURACIL 6-ETHYL-5-TETRADECYL-2-THIOURACIL AURORA KA-398 BUTTPARK 56\40-54 6-methyl-5-(2-propynyl)-2-thioxo-2,3-dihydro-4(1H)-pyrimidinone BUTTPARK 128\40-96 AURORA 12615 ETHYL (6-METHYL-4-OXO-2-THIOXO-1,2,3,4-TETRAHYDROPYRIMIDIN-5-YL)ACETATE 7-AMINO-4-OXO-5-PHENYL-2-THIOXO-1,3,5,8-TETRAHYDRO-8-OXAQUINAZOLINE-6-CARBONITRILE BUTTPARK 57\40-61 SPECS AB-321/43278427 5-BUTYL-6-HYDROXY-2-THIOXO-2,3-DIHYDRO-1H-PYRIMIDIN-4-ONE BUTTPARK 114\40-13 5-BENZYL-6-HYDROXY-2-THIOXO-2,3-DIHYDRO-1H-PYRIMIDIN-4-ONE BUTTPARK 114\40-12 SPECS AB-321/43278426

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