CAS 75028-24-9

(αZ)-5-Amino-α-(ethoxyimino)-1,2,4-thiadiazole-3-acetic acid

Description:

(αZ)-5-Amino-α-(ethoxyimino)-1,2,4-thiadiazole-3-acetic acid is a chemical compound characterized by its unique structure, which includes a thiadiazole ring, an amino group, and an ethoxyimino substituent. This compound typically exhibits properties associated with both acidic and basic functionalities due to the presence of the carboxylic acid group and the amino group, allowing it to participate in various chemical reactions, including protonation and deprotonation. The thiadiazole moiety contributes to its potential biological activity, making it of interest in pharmaceutical research. Its solubility in polar solvents is likely due to the presence of the carboxylic acid and amino groups, which can engage in hydrogen bonding. Additionally, the ethoxyimino group may influence its reactivity and stability. Overall, this compound's characteristics suggest potential applications in medicinal chemistry, particularly in the development of agrochemicals or pharmaceuticals, although specific biological activities would require further investigation.

Formula: C₆H₈N₄O₃S

InChI: InChI=1S/C6H8N4O3S/c1-2-13-9-3(5(11)12)4-8-6(7)14-10-4/h2H2,1H3,(H,11,12)(H2,7,8,10)/b9-3-

InChI key: InChIKey=UFTDZEXQFNFPFR-OQFOIZHKSA-N

SMILES: C(\C(O)=O)(=N\OCC)/C=1N=C(N)SN1

Synonyms:

• (Z)-5-Amino-alpha-(ethoxyimino)-1,2,4-thiadiazole-3-acetic acid
• (αZ)-5-Amino-α-(ethoxyimino)-1,2,4-thiadiazole-3-acetic acid
• 1,2,4-Thiadiazole-3-acetic acid, 5-amino-α-(ethoxyimino)-, (Z)-
• 1,2,4-Thiadiazole-3-acetic acid, 5-amino-α-(ethoxyimino)-, (αZ)-
• Atde
• Ceftazidime Norlin Intermediates
• Ceftaroline Fosamil Intermediate 2
• (Z)-2-(5-Amino-1,2,4-thiadiazol-3-yl)-2-ethoxyiminoacetic acid CAS RN 75028-24-9
• -2-(5-Amino-1,2,4-thiadiazol-3-yl)
• -2-(ethoxyimino)
• Sodium 1-(2-hydroxyethyl)-1H-tetrazol-5-ylthiolate，(Z)-2-(5-AMino-1,2,4-thiadiazol-3-yl)-2- ethoxyiMinoacetic acid
• (Z)-5-Amino-alpha-(ethoxyimino)-1
• 4-thiadiazole-3-acetic acid
• (Z)-2-(5-AMino-1,2,4-thiadiazol-3-yl)-2-ethoxyiMinoacetic acid
• (Z)-2-(5-Amino-1,2,4-thiadiazol-3-yl)-2-ethoxyiminoacetic acid
• 2-(5-Amino-1,2,4-thiadiazol-3-yl)-2-ethoxyiminoacetic acid
• (Z)-2-(5-Amino-1,2,4-thiadiazol-3-yl)-2-(ethoxyimino)acetic
• (2Z)-(ethoxyiMino)-2-(5-aMino-1,2,4-thiadiazol-3-yl)-acetic acid

(Z)-2-(5-Amino-1,2,4-thiadiazol-3-yl)-2-(ethoxyimino)acetic acid

CAS: 75028-24-9

Formula: C₆H₈N₄O₃S

Purity: 98%

Color and Shape: Solid

Molecular weight: 216.2177

Ref: IN-DA005RLG

(Z)-2-(5-AMino-1,2,4-thiadiazol-3-yl)-2-ethoxyiMinoacetic acid

CAS: 75028-24-9

(Z)-2-(5-AMino-1,2,4-thiadiazol-3-yl)-2-ethoxyiMinoacetic acid

Purity: 98%

Molecular weight: 216.22g/mol

Ref: 54-OR80250

(Z)-2-(5-Amino-1,2,4-thiadiazol-3-yl)-2-(ethoxyimino)acetic acid

CAS: 75028-24-9

(Z)-2-(5-Amino-1,2,4-thiadiazol-3-yl)-2-(ethoxyimino)acetic acid is a synthetic compound that can be used as an antibiotic. It is synthesized from acetonitrile and phosphorus oxychloride in the presence of hydroxyl groups. This reaction yields a mixture of amides and cyanoacetamide derivatives. The amides are then converted to their respective alkyl chlorides with methyl iodide, which are then reacted with dimethyl acetylenedicarboxylate to form the desired product. The final step is to hydrolyze the ester group with hydrochloric acid to yield (Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(ethoxyimino)acetic acid. This chemical has been shown to have antibacterial properties against some strains of bacteria such as

Formula: C₆H₈N₄O₃S

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 216.22 g/mol

Ref: 3D-FA33064

(Z)-2-(5-Amino-1,2,4-thiadiazol-3-yl)-2-(ethoxyimino)acetic acid

CAS: 75028-24-9

Formula: C₆H₈N₄O₃S

Purity: 95%

Color and Shape: Solid

Molecular weight: 216.22

Ref: 10-F210978

(Z)-2-(5-Amino-1,2,4-thiadiazol-3-yl)-2-(ethoxyimino)acetic Acid

CAS: 75028-24-9

Formula: C₆H₈N₄O₃S

Molecular weight: 216.22

Ref: ST-EA-CP-C138025