6-PHENYL-2,3-DIHYDROIMIDAZO[2,1-B][1,3]THIAZOLE-5-CARBALDEHYDE

Base Information

• Chemical Name: 6-PHENYL-2,3-DIHYDROIMIDAZO[2,1-B][1,3]THIAZOLE-5-CARBALDEHYDE
• CAS No.: 75224-64-5
• Molecular Formula: C12H10N2OS
• Molecular Weight: 230.29
• Hs Code.: 2934100090
• Mol file: 75224-64-5.mol

Synonyms:6-Phenyl-2,3-dihydroimidazo[2,1-b]thiazole-5-carboxaldehyde;

Chemical Property of 6-PHENYL-2,3-DIHYDROIMIDAZO[2,1-B][1,3]THIAZOLE-5-CARBALDEHYDE

Chemical Property:

• Vapor Pressure: 6.52E-10mmHg at 25°C
• Melting Point: 122-124℃
• Refractive Index: 1.715
• Boiling Point: 494.3 °C at 760 mmHg
• Flash Point: 252.8 °C
• PSA: 60.19000
• Density: 1.37 g/cm³
• LogP: 2.46830
• Sensitive.: Air Sensitive

Purity/Quality:

99%, ^*data from raw suppliers

6-Phenyl-2,3-dihydroimidazo[2,1-b]thiazole-5-carbaldehyde ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of 6-PHENYL-2,3-DIHYDROIMIDAZO[2,1-B][1,3]THIAZOLE-5-CARBALDEHYDE

There total 3 articles about 6-PHENYL-2,3-DIHYDROIMIDAZO[2,1-B][1,3]THIAZOLE-5-CARBALDEHYDE 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: 87.0%

2,3-diidro-6-fenilimidazo<2,1-b>tiazolo (4335-28-8) + N,N-dimethyl-formamide (68-12-2,33513-42-7) → 2,3-diidro-5-formil-6-fenilimidazo<2,1-b>tiazolo (75224-64-5)

Guidance literature:

With Vilsmeier reagent; In pyridine; chloroform; for 24h;

Reference yield: 22.0%

2,3-diidro-5-metil-6-fenilimidazo<2,1-b>tiazolo (75224-70-3) → 2,3-diidro-5-formil-6-fenilimidazo<2,1-b>tiazolo (75224-64-5)

Guidance literature:

With selenium(IV) oxide; In 1,4-dioxane; for 8h;

Reference yield:

2-bromo-1-phenyl-1-propanone (2114-00-3) → 2,3-diidro-5-formil-6-fenilimidazo<2,1-b>tiazolo (75224-64-5)

Guidance literature:

Multi-step reaction with 2 steps

1: 1.) ethanol, reflux, 15 h; 2.) ether, 24 h

2: 22 percent / SeO₂ / dioxane / 8 h

With selenium(IV) oxide; In 1,4-dioxane;

upstream raw materials:

2,3-diidro-6-fenilimidazo<2,1-b>tiazolo

N,N-dimethyl-formamide

2,3-diidro-5-metil-6-fenilimidazo<2,1-b>tiazolo

2-bromo-1-phenyl-1-propanone

Downstream raw materials:

5-((E)-2-Nitro-vinyl)-6-phenyl-2,3-dihydro-imidazo[2,1-b]thiazole

Dimethylamino-acetic acid [1-(6-phenyl-2,3-dihydro-imidazo[2,1-b]thiazol-5-yl)-meth-(E)-ylidene]-hydrazide

4-[(E)-2-(6-phenyl-2,3-dihydroimidazo[2,1-b][1,3]thiazol-5-yl)vinyl]pyrimidin-2-amine

6-Phenyl-2,3-dihydro-imidazo[2,1-b]thiazole-5-carbonitrile

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