Ethyl 2-amino-4-methylthiazole-5-carboxylate

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Products Intro: Product Name:ethyl 2-amino-4-methylthiazole-5-carboxylate
CAS:7210-76-6
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CAS:7210-76-6
Purity:98%(Min,HPLC) Package:100g;1kg;5kg,10kg,25kg,50kg
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CAS:7210-76-6
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Products Intro: Product Name:Ethyl 2-amino-4-methylthiazole-5-carboxylate
CAS:7210-76-6
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-03484

Ethyl 2-amino-4-methylthiazole-5-carboxylate manufacturers

Ethyl 2-amino-4-methylthiazole-5-carboxylate Basic information
Product Name:Ethyl 2-amino-4-methylthiazole-5-carboxylate
Synonyms:OTAVA-BB BB0108540072;TIMTEC-BB SBB000257;JR-6608, Ethyl 2-amino-4-methylthiazole-5-carboxylate, 97%;BUTTPARK 34\01-17;ASISCHEM Y51232;IFLAB-BB F1920-0015;ETHYL 2-AMINO-4-METHYL-1,3-THIAZOLE-5-CARBOXYLATE;ETHYL 2-AMINO-4-METHYLTHIAZOLE-5-CARBOXYLATE
CAS:7210-76-6
MF:C7H10N2O2S
MW:186.23
EINECS:628-116-2
Product Categories:API intermediates;Building Blocks;Heterocyclic Building Blocks;Amines;blocks;Carboxes;Thiazoles
Mol File:7210-76-6.mol
Ethyl 2-amino-4-methylthiazole-5-carboxylate Structure
Ethyl 2-amino-4-methylthiazole-5-carboxylate Chemical Properties
Melting point 176-180 °C(lit.)
Boiling point 313.1±22.0 °C(Predicted)
density 1.283±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
solubility DMF: 20 mg/ml; DMSO: 20 mg/ml; Ethanol: 20 mg/ml; Ethanol:PBS pH 7.2 (1:1): 0.5 mg/ml
form powder to crystal
pka3.90±0.10(Predicted)
color White to Almost white
Water Solubility insoluble
InChIInChI=1S/C7H10N2O2S/c1-3-11-6(10)5-4(2)9-7(8)12-5/h3H2,1-2H3,(H2,8,9)
InChIKeyWZHUPCREDVWLKC-UHFFFAOYSA-N
SMILESS1C(C(OCC)=O)=C(C)N=C1N
CAS DataBase Reference7210-76-6(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 36/37/38-22
Safety Statements 26-36-36/37/39-22
WGK Germany 3
HazardClass IRRITANT
HS Code 29349990
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
ALFA English
Ethyl 2-amino-4-methylthiazole-5-carboxylate Usage And Synthesis
Chemical Propertiesoff-white powder
UsesEthyl 2-amino-4-methylthiazole-5-carboxylate is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
Synthesis
Carbamimidothioic acid

17356-08-0

Ethyl 2-chloroacetoacetate

609-15-4

Ethyl 2-amino-4-methylthiazole-5-carboxylate

7210-76-6

Thiourea (2.55 g, 0.033 mol, 1.1 eq.) was added to a solution of ethyl 2-chloro-3-oxobutanoate (5 g, 0.030 mol, 1 eq.) in ethanol (25 mL) at 25 °C. The reaction mixture was heated to reflux and kept for 3 hours. Upon completion of the reaction, the reaction mixture was slowly cooled to 25 °C under continuous stirring to induce precipitation of the product as a white solid. The precipitated solid was collected by filtration through a Büchner funnel and dried under vacuum to afford ethyl 2-amino-4-methylthiazole-5-carboxylate (4.8 g, 64% yield) as a final fine white powder.

References[1] Patent: CN108570017, 2018, A. Location in patent: Paragraph 0030; 0031; 0033; 0035; 0037
[2] Chemical Biology and Drug Design, 2016, vol. 87, # 4, p. 508 - 516
[3] Patent: CN102942565, 2016, B. Location in patent: Paragraph 0028-0031; 0087-0088
[4] Archiv der Pharmazie, 2017, vol. 350, # 2,
[5] Acta Poloniae Pharmaceutica - Drug Research, 2017, vol. 74, # 6, p. 1699 - 1709
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