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60846-15-3

60846-15-3 Structure

60846-15-3 Structure
IdentificationBack Directory
[Name]

ETHYL 2-(2-AMINOTHIAZOLE-4-YL)-2-METHOXYIMINOACETATE
[CAS]

60846-15-3
[Synonyms]

ATE
(EZ)-(2-aminothiazoL
)-α-methoxyiminoacetate
2-amino-α-(methoxyimino)-, ethyl ester
Ethyl 2-amino-(methoxy imino)-4-thiazoleacetate
ethyl 2-amino-alpha-(methoxyimino)thiazol-4-acetate
Ethyl2-(2-amino-4-thiazolyl)-2-(methoxyimino)acetate
ETHYL 2-(2-AMINOTHIAZOLE-4-YL)-2-METHOXYIMINOACETATE
ethyl (EZ)-(2-aminothiazol-4-yl)-α-methoxyiminoacetate
ETHYL (Z)-2-(2-AMINO-4-THIAZOLYL)-2-METHOXYIMINOACETATE
ETHYL-2-METHOXY-AMINO-2-(2-AMINO-THIAZOLE-4-YL) ACETATE
ETHYL-2-(2-AMINO-4-THIAZOLYL)-2-(METHOXY IMINO) ACEATATE
4-THIAZOLEACETICACID,2-AMINO-A-(METHOXYIMINO)-,ETHYLESTER
2-Amino-α-(methoxyimino)-4-thiazoleacetic acid ethyl ester
4-Thiazoleacetic acid, 2-amino-α-(methoxyimino)-, ethyl ester
2-AMINO-ALPHA-(METHOXYIMINO)-4-THIAZOLEACETIC ACID ETHYL ESTER
ETHYL (2E)-2-(2-AMINO-1,3-THIAZOL-4-YL)-2-METHOXYIMINO-ACETATE
4-THIAZOLEACETIC ACID, 2-AMINO-ALPHA-(METHOXYIMINO)-, ETHYL ESTER
(2Z)-2-(2-amino-4-thiazolyl)-2-methoxyiminoacetic acid ethyl ester
4-THIAZOLEACETIC ACID, 2-AMINO-ALPHA-(METHOXYIMINO)-, ETHYL ESTER, (AZ)-
[EINECS(EC#)]

262-470-5
[Molecular Formula]

C8H11N3O3S
[MDL Number]

MFCD00010588
[MOL File]

60846-15-3.mol
[Molecular Weight]

229.26
Chemical PropertiesBack Directory
[Melting point ]

162-164 °C(lit.)
[Boiling point ]

363.4±34.0 °C(Predicted)
[density ]

1.41±0.1 g/cm3(Predicted)
[pka]

2.57±0.10(Predicted)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-37/39
[WGK Germany ]

3
Hazard InformationBack Directory
[Chemical Properties]

White crystals. Melting point 162-164°C (155-160°C).
[Uses]

Ethyl 2-(2-aminothiazole-4-yl)-2-methoxyiminoacetate is an intermediates (side chains) of third-generation cephalosporins, such as cefmenoxime, ceftriaxone, ceftriaxone, and cefotaxime.
[Synthesis]

Ethyl 2-(2-aminothiazole-4-yl)-2-methoxyiminoacetate can be obtained by oximation, methylation, bromination and cyclization with ethyl acetoacetate.
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