CAS 118969-27-0

4,5-DIHYDRO-2[6-AMINO-2-BENZTHIAZOLYL]-4-THIAZOLE CARBOXYLIC ACID

Description:

4,5-Dihydro-2[6-amino-2-benzothiazolyl]-4-thiazole carboxylic acid is a chemical compound characterized by its complex structure, which includes a thiazole ring and a benzothiazole moiety. This compound typically exhibits properties associated with heterocyclic compounds, such as potential biological activity due to the presence of nitrogen and sulfur atoms in its rings. The amino group in the benzothiazole structure may contribute to its reactivity and solubility in polar solvents. The carboxylic acid functional group suggests acidic properties, allowing for potential interactions in biological systems, such as hydrogen bonding and ionic interactions. This compound may be of interest in medicinal chemistry, particularly for its potential pharmacological applications. Its specific characteristics, such as melting point, solubility, and spectral properties, would depend on the purity and specific conditions under which it is studied. As with many heterocycles, it may also exhibit unique electronic properties due to the conjugation within its structure.

Formula: C₁₁H₉N₃O₂S₂

InChI: InChI=1/C11H9N3O2S2/c12-5-1-2-6-8(3-5)18-10(13-6)9-14-7(4-17-9)11(15)16/h1-3,7H,4,12H2,(H,15,16)

SMILES: c1cc2c(cc1N)sc(C1=NC(CS1)C(=O)O)n2

Synonyms:

• ADL
• 6-Amino-6-Deoxyluciferin
• 6-Amino-D-Luciferin
• 6-Amino Luciferin
• 6-Amino-6-Deoxyluciferin (Adl)
• 2-(6-Amino-1,3-Benzothiazol-2-Yl)-4,5-Dihydro-1,3-Thiazole-4-Carboxylic Acid

6-Amino-6-deoxyluciferin

CAS: 118969-27-0

6-Amino-6-deoxyluciferin is a synthetic analog of luciferin. It is used as a substrate for bacterial luciferase and in immunoassays to detect neutrophils, infectious diseases, and various protease activities. 6-Amino-6-deoxyluciferin is synthesized by the condensation of an amide with a hydroxyl group from acetaldehyde. This reaction requires the use of a coupling agent such as dicyclohexylcarbodiimide or 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC), which are often used to form amides from carboxylic acids and amines. The conjugation of 6-amino-6-deoxyluciferin with antibodies can be accomplished by chemical crosslinking methods, such as glutaraldehyde, which react thiol groups on the antibody

Formula: C₁₁H₉N₃O₂S₂

Purity: Min. 95%

Color and Shape: Yellow Solid

Molecular weight: 279.34 g/mol

Ref: 3D-FA36330