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ChemicalBook >  Product Catalog >  Biochemical Engineering >  Amino Acids and Derivatives >  Amino acid esters >  Ethyl 2-amino-1,3-thiazole-4-carboxylate

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
  • pharmacetical
  • Esters
  • Thiazoles, Isothiazoles &Benzothiazoles
  • Pharmaceutical raw materials
  • Amines
  • blocks
  • Carboxes
  • Thiazoles
  • Amino Acids and Derivatives
  • Heterocycle intermediates
  • API
  • Thiazoles, Isothiazoles & Benzothiazoles
  • 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.

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