CAS 5398-36-7

Etil 2-ammino-4-tiazolcarbossilato

Descrizione:

Etil 2-ammino-4-tiazolcarbossilato è un composto organico caratterizzato dal suo anello di tiazolo, che è una struttura eterociclica a cinque membri contenente zolfo e azoto. Questo composto presenta un gruppo funzionale di estere etilico, contribuendo alla sua reattività e solubilità nei solventi organici. La presenza del gruppo amminico (-NH2) aumenta il suo potenziale per formare legami idrogeno, rendendolo un intermedio versatile nella sintesi organica. Etil 2-ammino-4-tiazolcarbossilato è spesso utilizzato nella sintesi di vari farmaci e agrochimici grazie alla sua attività biologica, in particolare nello sviluppo di agenti antimicrobici e antinfiammatori. La sua struttura molecolare consente varie reazioni di sostituzione, rendendolo un blocco di costruzione prezioso nella chimica medicinale. Inoltre, è importante maneggiare questo composto con cura, poiché può comportare rischi per la salute se ingerito o inalato, e devono essere seguiti i protocolli di sicurezza adeguati durante il suo utilizzo in ambienti di laboratorio.

Formula: C₆H₈N₂O₂S

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

InChI key: InChIKey=XHFUVBWCMLLKOZ-UHFFFAOYSA-N

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

Sinonimi:

• 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

Formula: C₆H₈N₂O₂S

Purezza: >98.0%(GC)(T)

Colore e forma: White to Orange to Green powder to crystal

Peso molecolare: 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

Formula: C₆H₈N₂O₂S

Purezza: 98%

Colore e forma: Powder, Pale cream to cream to pale yellow

Peso molecolare: 172.20

Ref: 02-H30634

Ethyl 2-aminothiazole-4-carboxylate

CAS: 5398-36-7

Formula: C₆H₈N₂O₂S

Purezza: 97%

Colore e forma: Solid

Peso molecolare: 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

Formula: C₆H₈N₂O₂S

Purezza: ≥95%

Colore e forma: yellow powder

Peso molecolare: 172.20g/mol

Ref: 54-OR10473

Ethyl 2-aminothiazole-4-carboxylate

CAS: 5398-36-7

Formula: C₆H₈N₂O₂S

Purezza: 97%

Colore e forma: Solid

Peso molecolare: 172.2

Ref: 10-F017326

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

Prodotto controllato

CAS: 5398-36-7

Formula: C₆H₈N₂O₂S

Colore e forma: Neat

Peso molecolare: 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.

Formula: C₆H₈N₂O₂S

Purezza: Min. 99.0 Area-%

Peso molecolare: 172.21 g/mol

Ref: 3D-FE43670

Acotiamide Impurity 3

CAS: 5398-36-7

Formula: C₆H₈N₂O₂S

Peso molecolare: 172.2

Ref: ST-EA-CP-A45005