220558
Ethyl 2-aminothiazole-4-acetate
99%
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About This Item
Empirical Formula (Hill Notation):
C7H10N2O2S
CAS Number:
Molecular Weight:
186.23
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
258-452-1
Beilstein/REAXYS Number:
139617
MDL number:
Product Name
Ethyl 2-aminothiazole-4-acetate, 99%
InChI key
SHQNGLYXRFCPGZ-UHFFFAOYSA-N
InChI
1S/C7H10N2O2S/c1-2-11-6(10)3-5-4-12-7(8)9-5/h4H,2-3H2,1H3,(H2,8,9)
SMILES string
CCOC(=O)Cc1csc(N)n1
assay
99%
mp
92-94 °C (lit.)
functional group
ester
Quality Level
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Application
Ethyl 2-aminothiazole-4-acetate was used in the synthesis of:
- bis (2-aminothiazole-4-acetato)aquazinc(II)
- dichloridobis[ethyl 2-(2-amino-1, 3-thiazol-4-yl) acetate-κ2O,N3]cadmium
- novel heteroaryl-containing benzamide derivatives
General description
Ethyl 2-aminothiazole-4-acetate is an organic ligand and possess strong coordination ability and display diverse coordination modes due to the presence of N, O coordination atoms.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
365.0 °F - closed cup
flash_point_c
185 °C - closed cup
ppe
Eyeshields, Gloves, type N95 (US)
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Lai-Jun Zhang et al.
Acta crystallographica. Section E, Structure reports online, 65(Pt 12), m1517-m1517 (2009-01-01)
In the title compound, [Zn(C(5)H(5)N(2)O(2)S)(2)(H(2)O)], the central Zn atom (2 site symmetry) is five-coordinated by two N and three O atoms [Zn-N = 2.047 (3) Å, Zn-O = 2.099 (2) and 1.974 (4) Å] in a distorted square-pyramidal geometry. Besides one O atom from a
Lai-Jun Zhang et al.
Acta crystallographica. Section E, Structure reports online, 68(Pt 6), m788-m789 (2012-06-22)
The asymmetric unit of the title compound, [CdCl(2)(C(7)H(10)N(2)O(2)S)(2)], contains two complex molecules with similar configurations. The Cd(II) atoms are each six-coordinated by two thiazole N and two carbonyl O atoms from the 2-(2-amino-1,3-thiazol-4-yl)acetate ligand, and by two Cl(-) anions in
Kaapjoo Park et al.
Bioorganic & medicinal chemistry, 22(7), 2280-2293 (2014-03-05)
Novel heteroaryl-containing benzamide derivatives were synthesized and screened using an in vitro assay measuring increases in glucose uptake and glucokinase activity stimulated by 10mM glucose in rat hepatocytes. From a library of synthesized compounds, 3-(4-methanesulfonylphenoxy)-N-[1-(2-methoxy-ethoxymethyl)-1H-pyrazol-3-yl]-5-(3-methyl pyridin-2-yl)-benzamide (19e) was identified as
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