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72054-60-5

72054-60-5 Structure

72054-60-5 Structure
IdentificationBack Directory
[Name]

METHYL 2-(2-AMINO-5-METHYL-1,3-THIAZOL-4-YL)ACETATE
[CAS]

72054-60-5
[Synonyms]

2-amino-5-ethoxycarbonyl-4-methylthiazole
5-CHLORO-1,2,3,4-TETRAHYDRO-[2,6]NAPHTHYRIDINE
methyl 2-(2-amino-5-methylthiazol-4-yl)acetate
METHYL (2-AMINO-5-METHYL-1,3-THIAZOL-4-YL)ACETATE
METHYL 2-(2-AMINO-5-METHYL-1,3-THIAZOL-4-YL)ACETATE
4-Thiazolecarboxylic acid, 2-amino-5-methyl-, ethyl ester
METHYL 2-(2-AMINO-5-METHYL-1,3-THIAZOL-4-YL)ACETATE###72054-60-5
[Molecular Formula]

C7H10N2O2S
[MDL Number]

MFCD00662517
[MOL File]

72054-60-5.mol
[Molecular Weight]

186.23
Chemical PropertiesBack Directory
[Melting point ]

111-113°C
[Boiling point ]

313.1±22.0 °C(Predicted)
[density ]

1.283±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Sealed in dry,2-8°C
[pka]

3.08±0.10(Predicted)
[Appearance]

Light yellow to yellow Solid
[InChI]

InChI=1S/C7H10N2O2S/c1-3-11-6(10)5-4(2)12-7(8)9-5/h3H2,1-2H3,(H2,8,9)
[InChIKey]

KTGUPAFUVGHOQS-UHFFFAOYSA-N
[SMILES]

S1C(C)=C(C(OCC)=O)N=C1N
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P264-P280-P302+P352-P321-P332+P313-P362-P305+P351+P338-P337+P313-P261-P271-P304+P340-P312-P403+P233-P405-P501
[HazardClass ]

IRRITANT
Spectrum DetailBack Directory
[Spectrum Detail]

METHYL 2-(2-AMINO-5-METHYL-1,3-THIAZOL-4-YL)ACETATE(72054-60-5)1HNMR
Hazard InformationBack Directory
[Synthesis]

Carbamimidothioic acid

17356-08-0

Ethyl 2-chloroacetoacetate

609-15-4

METHYL 2-(2-AMINO-5-METHYL-1,3-THIAZOL-4-YL)ACETATE

72054-60-5

Step 2: Synthesis of ethyl 2-amino-5-methylthiazole-4-carboxylate Thiourea (47 g, 616.83 mmol) was added to a solution of ethyl 2-chloro-3-oxobutanoate (100 g, 577.19 mmol) in ethanol (1000 mL). The resulting mixture was stirred and reacted under reflux conditions for 2 hours. Upon completion of the reaction, the reaction mixture was cooled to room temperature in a water/ice bath. The precipitate was collected by filtration to give 105 g (93% yield) of ethyl 2-amino-5-methylthiazole-4-carboxylate as a light yellow solid.

[References]

[1] Patent: US2008/139558, 2008, A1. Location in patent: Page/Page column 51
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