CAS 53266-94-7

Ethyl 2-amino-4-thiazoleacetate

Description:

Ethyl 2-amino-4-thiazoleacetate, with the CAS number 53266-94-7, is an organic compound characterized by its thiazole ring, which is a five-membered heterocyclic structure containing sulfur and nitrogen. This compound features an ethyl ester functional group, contributing to its solubility in organic solvents. The presence of the amino group (-NH2) enhances its reactivity, making it a potential candidate for various chemical reactions, including those involving nucleophilic substitution. Ethyl 2-amino-4-thiazoleacetate is often studied for its biological activity, as thiazole derivatives are known to exhibit a range of pharmacological properties, including antimicrobial and anti-inflammatory effects. The compound's molecular structure allows for potential interactions with biological targets, making it of interest in medicinal chemistry. Additionally, its synthesis typically involves straightforward organic reactions, making it accessible for research and development purposes. Overall, this compound exemplifies the diverse applications of thiazole derivatives in both synthetic and medicinal chemistry.

Formula: C₇H₁₀N₂O₂S

InChI: InChI=1S/C7H10N2O2S/c1-2-11-6(10)3-5-4-12-7(8)9-5/h4H,2-3H2,1H3,(H2,8,9)

InChI key: InChIKey=SHQNGLYXRFCPGZ-UHFFFAOYSA-N

SMILES: C(C(OCC)=O)C=1N=C(N)SC1

Synonyms:

• (2-Amino-1,3-thiazol-4-yl)acetic acid ethyl ester
• (2-Amino-4-thiazolyl)acetic acid ethyl ester
• (2-Amino-thiazole-4-yl)acetic acid ethyl ester
• 2-(2-Aminothiazol-4-yl)acetic acid ethyl ester
• 2-Amino-4-(carbethoxymethyl)thiazole
• 2-Amino-4-(ethoxycarbonylmethyl)-1,3-thiazole
• 2-Amino-4-[(ethoxycarbonyl)methyl]thiazole
• 2-Amino-4-thiazoleacetic acid ethyl ester
• 4-Thiazoleacetic acid, 2-amino-, ethyl ester
• Eata
• Ethyl (2-Amino-1,3-Thiazol-4-Yl)Acetate
• Ethyl 2-(2-amino-1,3-thiazol-4-yl)acetate
• Ethyl 2-(2-aminothiazol-4-yl) acetate
• Ethyl 2-aminothiazol-4-yl-acetate
• Ethyl 2-aminothiazol-4-ylacetate

Ethyl (2-Amino-4-thiazolyl)acetate

CAS: 53266-94-7

Formula: C₇H₁₀N₂O₂S

Purity: >98.0%(GC)(T)

Color and Shape: Light yellow to Brown powder to crystal

Molecular weight: 186.23

Ref: 3B-A0955

Ethyl 2-Amino-4-Thiazoleacetate

CAS: 53266-94-7

Formula: C₇H₁₀N₂O₂S

Purity: 97%

Color and Shape: Solid

Molecular weight: 186.2315

Ref: IN-DA0034U7

Ethyl 2-(2-aminothiazol-4-yl)acetate

CAS: 53266-94-7

Formula: C₇H₁₀N₂O₂S

Molecular weight: 186.23

Ref: 7W-GK4296

ethyl 2-(2-amino-1,3-thiazol-4-yl)acetate

CAS: 53266-94-7

ethyl 2-(2-amino-1,3-thiazol-4-yl)acetate

Purity: 98%

Molecular weight: 186.23g/mol

Ref: 54-OR28617

(2-Aminothiazol-4-yl)acetic acid ethyl ester

CAS: 53266-94-7

Formula: C₇H₁₀N₂O₂S

Purity: 97%

Color and Shape: Solid, No data available.

Molecular weight: 186.23

Ref: 10-F014155

Ethyl 2-Amino-4-thiazoleacetate

Controlled Product

CAS: 53266-94-7

Formula: C₇H₁₀N₂O₂S

Color and Shape: Neat

Molecular weight: 186.23

Ref: TR-E899330

Ethyl 2-amino-4-thiazoleacetate

CAS: 53266-94-7

Ethyl 2-amino-4-thiazoleacetate is a supramolecular molecule that has the potential to be an anticancer agent. It inhibits the growth of tumor cells by binding to tyrosinase and hydrogen-bonding with chloride ions in solution. Ethyl 2-amino-4-thiazoleacetate also binds to a metal ion, such as zinc, which is important for biological functions. When it binds to these metals, it inhibits the enzyme hepg2 cell, which is involved in the synthesis of protein from RNA. Inhibition of this enzyme leads to decreased production of cytokines, which are molecules that regulate immune responses. This drug also has inhibitory activities against oral cephalosporins when used in combination with other drugs.

Formula: C₇H₁₀N₂O₂S

Purity: Min. 95%

Molecular weight: 186.23 g/mol

Ref: 3D-FE10858

Mirabegron Impurity 53

CAS: 53266-94-7

Formula: C₇H₁₀N₂O₂S

Molecular weight: 186.23

Ref: ST-EA-CP-M21059