CAS 5398-36-7

Etil 2-amino-4-tiazolcarboxilato

Descripción:

Etil 2-amino-4-tiazolcarboxilato es un compuesto orgánico caracterizado por su anillo de tiazol, que es una estructura heterocíclica de cinco miembros que contiene azufre y nitrógeno. Este compuesto presenta un grupo funcional de éster etílico, lo que contribuye a su reactividad y solubilidad en disolventes orgánicos. La presencia del grupo amino (-NH2) mejora su potencial para formar enlaces de hidrógeno, lo que lo convierte en un intermediario versátil en la síntesis orgánica. Etil 2-amino-4-tiazolcarboxilato se utiliza a menudo en la síntesis de varios fármacos y agroquímicos debido a su actividad biológica, particularmente en el desarrollo de agentes antimicrobianos y antiinflamatorios. Su estructura molecular permite diversas reacciones de sustitución, lo que lo convierte en un bloque de construcción valioso en la química medicinal. Además, es importante manejar este compuesto con cuidado, ya que puede representar riesgos para la salud si se ingiere o inhala, y se deben seguir los protocolos de seguridad adecuados durante su uso en entornos de laboratorio.

Fórmula: C₆H₈N₂O₂S

InChI: InChI=1S/C6H8N2O2S/c1-2-10-5(9)4-3-11-6(7)8-4/h3H,2H2,1H3,(H2,7,8)

Clave InChI: InChIKey=XHFUVBWCMLLKOZ-UHFFFAOYSA-N

SMILES: C(OCC)(=O)C1=CSC(N)=N1

Sinónimos:

• 2-Amino-1,3-Thiazole-4-Carboxylate
• 2-Amino-1,3-thiazole-4-carboxylic acid ethyl ester
• 2-Amino-4-(ethoxycarbonyl)-1,3-thiazole
• 2-Amino-4-Thiazolecarboxylic acid ethyl ester
• 2-Amino-4-ethoxycarbonylthiazole
• 2-Aminothiazol-4-carboxylic acid ethyl ester
• 2-Aminothiazole-4-carboxylic Acid Ethyl Ester
• 2-Imino-2,3-dihydro-thiazole-4-carboxylic acid ethyl ester
• 4-Thiazolecarboxylic acid, 2-amino-, ethyl ester
• Ethyl 2-amino-1,3-thiazole-4-carboxylate
• Ethyl 2-amino-4-thiazolecarboxylate
• NSC 43547

Ethyl 2-Aminothiazole-4-carboxylate

CAS: 5398-36-7

Fórmula: C₆H₈N₂O₂S

Pureza: >98.0%(GC)(T)

Forma y color: White to Orange to Green powder to crystal

Peso molecular: 172.20

Ref: 3B-E1215

Ethyl 2-aminothiazole-4-carboxylate, 98%

CAS: 5398-36-7

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci

Fórmula: C₆H₈N₂O₂S

Pureza: 98%

Forma y color: Powder, Pale cream to cream to pale yellow

Peso molecular: 172.20

Ref: 02-H30634

Ethyl 2-aminothiazole-4-carboxylate

CAS: 5398-36-7

Fórmula: C₆H₈N₂O₂S

Pureza: 97%

Forma y color: Solid

Peso molecular: 172.2049

Ref: IN-DA003Q38

Ethyl 2-amino-1,3-thiazole-4-carboxylate

CAS: 5398-36-7

Ethyl 2-amino-1,3-thiazole-4-carboxylate

Fórmula: C₆H₈N₂O₂S

Pureza: ≥95%

Forma y color: yellow powder

Peso molecular: 172.20g/mol

Ref: 54-OR10473

Ethyl 2-aminothiazole-4-carboxylate

CAS: 5398-36-7

Fórmula: C₆H₈N₂O₂S

Pureza: 97%

Forma y color: Solid

Peso molecular: 172.2

Ref: 10-F017326

Ethyl 2-Amino-1,3-thiazole-4-carboxylate

Producto controlado

CAS: 5398-36-7

Fórmula: C₆H₈N₂O₂S

Forma y color: Neat

Peso molecular: 172.2

Ref: TR-E678465

Ethyl 2-amino-thiazole-4-carboxylate

CAS: 5398-36-7

Ethyl 2-amino-thiazole-4-carboxylate (ETAC) is an inhibitor of protein synthesis. It binds to the dna and inhibits transcription, leading to cell death by inhibiting the production of proteins vital for cell division. ETAC has been shown to have cytotoxic activity against cancer cells and hemolytic activity. It also has a strong fluorescence probe property, which may be used in cancer diagnosis. ETAC can inhibit protein synthesis in cells that are resistant to other antimicrobial agents and platinum-based chemotherapy, making it a potential treatment for these infections. The pharmacokinetic properties of ETAC are not well studied but it is excreted through urine, suggesting that it is hydrophilic and may be metabolized with glucuronidation or sulfation. The molecular modeling study suggests that the hydrogen bond between ETAC and the dna phosphate group may explain its inhibitory effects on DNA synthesis.

Fórmula: C₆H₈N₂O₂S

Pureza: Min. 99.0 Area-%

Peso molecular: 172.21 g/mol

Ref: 3D-FE43670

Acotiamide Impurity 3

CAS: 5398-36-7

Fórmula: C₆H₈N₂O₂S

Peso molecular: 172.2

Ref: ST-EA-CP-A45005