Basic information Uses Safety Supplier Related

Methyl 2-amino-4-methylthiazole-5-carboxylate

Basic information Uses Safety Supplier Related

Methyl 2-amino-4-methylthiazole-5-carboxylate Basic information

Product Name:
Methyl 2-amino-4-methylthiazole-5-carboxylate
Synonyms:
  • 2-AMINO-4-METHYL-THIAZOLE-5-CARBOXYLIC ACID METHYL ESTER
  • METHYL 2-AMINO-4-METHYL-1,3-THIAZOLE-5-CARBOXYLATE
  • METHYL 2-AMINO-4-METHYLTHIAZOLE-5-CARBOXYLATE
  • CHEMBRDG-BB 4142897
  • BUTTPARK 76\07-67
  • ART-CHEM-BB B000344
  • AKOS B000344
  • 2-Amino-4-methylthiazole-5-methyl formate
CAS:
3829-80-9
MF:
C6H8N2O2S
MW:
172.2
EINECS:
672-079-5
Mol File:
3829-80-9.mol
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Methyl 2-amino-4-methylthiazole-5-carboxylate Chemical Properties

Melting point:
171-174 °C
Boiling point:
301.3±22.0 °C(Predicted)
Density 
1.339±0.06 g/cm3(Predicted)
storage temp. 
2-8°C, protect from light
pka
3.83±0.10(Predicted)
form 
solid
color 
Yellow
InChI
InChI=1S/C6H8N2O2S/c1-3-4(5(9)10-2)11-6(7)8-3/h1-2H3,(H2,7,8)
InChIKey
TYUGYIMCRDPMPJ-UHFFFAOYSA-N
SMILES
S1C(C(OC)=O)=C(C)N=C1N
CAS DataBase Reference
3829-80-9(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
HazardClass 
IRRITANT
HS Code 
2934100090
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Methyl 2-amino-4-methylthiazole-5-carboxylate Usage And Synthesis

Uses

Methyl 2-amino-4-methylthiazole-5-carboxylate is a useful research chemical.

Chemical Properties

white crysta

Synthesis

105-45-3

17356-08-0

3829-80-9

GENERAL METHODS: A mixture of methyl acetoacetate (0.5 mmol), thiourea (0.5 mmol), iodine (0.5 mmol), DMSO (2 mL), and MMT-K10 (20 mg) was reacted at 80 °C with stirring. The reaction progress was monitored by TLC (unfolding agent: petroleum ether/ethyl acetate, 4:1). Upon completion of the reaction, the catalyst was separated by filtration and the solvent was subsequently removed under reduced pressure. The crude product was dissolved in hot water and extracted with ether (3 x 30 mL), and the pH of the aqueous phase was adjusted to 9-10 with ammonia to precipitate the solid product. Finally, the resulting precipitate was recrystallized from ethanol to give methyl 2-amino-4-methylthiazole-5-carboxylate.

References

[1] RSC Advances, 2016, vol. 6, # 69, p. 64749 - 64755
[2] Research on Chemical Intermediates, 2016, vol. 42, # 12, p. 8175 - 8183
[3] Advanced Synthesis and Catalysis, 2018, vol. 360, # 8, p. 1584 - 1589
[4] Monatshefte fur Chemie, 2017, vol. 148, # 4, p. 745 - 749
[5] Journal of Molecular Structure, 2017, vol. 1144, p. 58 - 65

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