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Ethyl 2-amino-1,3-thiazole-4-carboxylate

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Ethyl 2-amino-1,3-thiazole-4-carboxylate Basic information

Product Name:
Ethyl 2-amino-1,3-thiazole-4-carboxylate
Synonyms:
  • 2-AMINO-1,3-THIAZOLE-4-CARBOXYLIC ACID ETHYL ESTER
  • 2-AMino-thiazol-4-carboxylic acid ethyl ester
  • Ethyl 2-aMino-thiazol-4-carboxylate
  • Ethyl 2-aMinothiazol-4-carboxylate
  • 2-aMino-4-thiazolecarboxylate
  • 2-Amino-4-(ethoxycarbonyl)-1,3-thiazole
  • Ethyl 2-AMinothiazole-4-carboxylate, 97+%
  • Ethyl 2-aminothiazole-4-carboxylate 96%
CAS:
5398-36-7
MF:
C6H8N2O2S
MW:
172.2
EINECS:
611-074-4
Product Categories:
  • amine| carboxylic ester
  • Building Blocks/Intermediates
  • Pharmaceutical raw materials
  • pharmacetical
  • Esters
  • Thiazoles, Isothiazoles &Benzothiazoles
  • Amines
  • blocks
  • Carboxes
  • Thiazoles
  • Thiazoles, Isothiazoles & Benzothiazoles
  • API
  • Heterocycle intermediates
  • Amino Acids and Derivatives
  • Heterocycles
  • bc0001
  • 5398-36-7
Mol File:
5398-36-7.mol
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Ethyl 2-amino-1,3-thiazole-4-carboxylate Chemical Properties

Melting point:
177 °C
Boiling point:
308.0±15.0 °C(Predicted)
Density 
1.336±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
DMSO (Slightly), Methanol (Slightly)
form 
Solid
pka
2.60±0.10(Predicted)
color 
Pale Beige
λmax
284nm(MeOH)(lit.)
InChI
InChI=1S/C6H8N2O2S/c1-2-10-5(9)4-3-11-6(7)8-4/h3H,2H2,1H3,(H2,7,8)
InChIKey
XHFUVBWCMLLKOZ-UHFFFAOYSA-N
SMILES
S1C=C(C(OCC)=O)N=C1N
CAS DataBase Reference
5398-36-7(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
36/37/38-22
Safety Statements 
24/25-36/37/39-26-22
WGK Germany 
nwg
HazardClass 
IRRITANT
HS Code 
29349990
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Ethyl 2-amino-1,3-thiazole-4-carboxylate Usage And Synthesis

Chemical Properties

white crystal powde

Uses

Ethyl 2-Amino-1,3-thiazole-4-carboxylate is a chemical reagent used in the preparation fo SAR thiazolamino arylaminopyrimidines as anaplastic lymphoma kinase inhibitors. As well as in the synthesis of 4-bicyclick piperadine derivatives as potent stearoyl-CoA desaturase (SCD1) inhibitors in the treatment of cancer.

Synthesis

70-23-5

17356-08-0

5398-36-7

GENERAL METHOD: A mixture of thiourea (1.2 mmol) and ethyl 3-bromopyruvate (1 mmol) in ethanol (2 mL) was reacted with stirring at 70°C for 1 hour. After completion of the reaction, the mixture was cooled to room temperature and subsequently poured into ice water. The precipitate precipitated was collected by filtration and dried to give the target product ethyl 2-aminothiazole-4-carboxylate. The products were characterized as follows: 6a (99% yield), white solid, melting point 150-152 °C (literature value 149-150 °C); 6b (100% yield), white solid, melting point 162-165 °C (literature value 163-164 °C); 6c (0.236 g, 93% yield), white solid, melting point 179-181 °C (literature value 180- 181°C); 6d (98% yield), white solid, melting point 203.6-204.2°C (literature value 204.0-204.5°C); 6e (94% yield), bright yellow solid, melting point 287-288°C (literature value 285-286°C); 6f (100% yield), white solid, melting point 172-174°C (literature value 172°C).

References

[1] Arkivoc, 2018, vol. 2018, # 7, p. 110 - 118
[2] Patent: CN104016944, 2016, B. Location in patent: Paragraph 0014-0015; 0040-0041
[3] Organic and Biomolecular Chemistry, 2012, vol. 10, # 30, p. 5764 - 5768
[4] Letters in Drug Design and Discovery, 2018, vol. 16, # 2, p. 160 - 173
[5] Patent: WO2007/146066, 2007, A2. Location in patent: Page/Page column 151-152

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