Thiazole orange

Base Information

• Chemical Name: Thiazole orange
• CAS No.: 107091-89-4
• Molecular Formula: C26H24N2O3S2
• Molecular Weight: 476.62
• European Community (EC) Number: 628-432-0
• UNII: 7UU5MK2XLQ
• DSSTox Substance ID: DTXSID20910233
• Wikidata: Q27123355
• ChEMBL ID: CHEMBL4094858
• Mol file: 107091-89-4.mol

Synonyms:thiazole orange

Chemical Property of Thiazole orange

Chemical Property:

• Melting Point: 270 °C
• PSA: 102.63000
• LogP: 5.30730
• Solubility.: DMSO: soluble
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 1
• Exact Mass: 476.12283498
• Heavy Atom Count: 33
• Complexity: 628

Purity/Quality:

98%Min ^*data from raw suppliers

ThiazoleOrange(90%) ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: CC1=CC=C(C=C1)S(=O)(=O)[O-].CN1C2=CC=CC=C2SC1=CC3=CC=[N+](C4=CC=CC=C34)C
• Isomeric SMILES: CC1=CC=C(C=C1)S(=O)(=O)[O-].CN\1C2=CC=CC=C2S/C1=C\C3=CC=[N+](C4=CC=CC=C34)C
• Uses: Thiazol Orange is a nucleic acid stain that has found applications in many different areas. Among others it is used for reticulocyte analysis and Plasmodium species analysis as well as labeling cancer cells. Thiazole orange-labeled DANN has been used fo Stains DNA or RNA in flow cytometry reticulocyte analysis, in agarose gels, in capillary electrophoresis. Thiazole Orange is a fluorescent DNA staining dye used for reticulocyte analysis. Dyes and metabolites.

Technology Process of Thiazole orange

There total 2 articles about Thiazole orange which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

C7H7O3S(1-)*C19H17N2S(1+)*C48H48N32O16 → thiazole orange (107091-89-4)

Guidance literature:

With amantadine hydrochloride; In water;

DOI:10.1039/c1cc12599k

Reference yield:

C7H7O3S(1-)*C19H17N2S(1+)*2C42H42N28O14 → thiazole orange (107091-89-4)

Guidance literature:

With amantadine hydrochloride; In water;

DOI:10.1039/c1cc12599k

Reference yield:

thiazole orange (107091-89-4) + cucurbit[7]uril → C19H17N2S(1+)*C7H7O3S(1-)*C42H42N28O14

Guidance literature:

With sodium chloride; In water;

DOI:10.1021/jp512802u

Refernces