2-(4-Nitrophenyl)Benzo[D]Imidazo[2,1-B]Thiazol-7-Ol

95%

Reagent Code: #220181
fingerprint
CAS Number 914224-34-3

science Other reagents with same CAS 914224-34-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 311.32 g/mol
Formula C₁₅H₉N₃O₃S
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in organic semiconductor materials due to its extended π-conjugated structure, enhancing electron transport in thin-film transistors.

Applied in fluorescence-based sensors for detecting metal ions like Cu²⁺ and Hg²⁺ in environmental and biological samples.

Serves as a key intermediate in synthesizing antitumor agents, particularly in developing kinase inhibitors.

Explored in photodynamic therapy research for its ability to generate reactive oxygen species under light exposure.

Incorporated into dye-sensitized solar cells as a sensitizer to improve light absorption and energy conversion efficiency.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,040.00
inventory 250mg
10-20 days ฿8,380.00
inventory 1g
10-20 days ฿16,740.00
inventory 5g
10-20 days ฿61,640.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-(4-Nitrophenyl)Benzo[D]Imidazo[2,1-B]Thiazol-7-Ol
No image available

Used in organic semiconductor materials due to its extended π-conjugated structure, enhancing electron transport in thin-film transistors.

Applied in fluorescence-based sensors for detecting metal ions like Cu²⁺ and Hg²⁺ in environmental and biological samples.

Serves as a key intermediate in synthesizing antitumor agents, particularly in developing kinase inhibitors.

Explored in photodynamic therapy research for its ability to generate reactive oxygen species under light exposure.

<

Used in organic semiconductor materials due to its extended π-conjugated structure, enhancing electron transport in thin-film transistors.

Applied in fluorescence-based sensors for detecting metal ions like Cu²⁺ and Hg²⁺ in environmental and biological samples.

Serves as a key intermediate in synthesizing antitumor agents, particularly in developing kinase inhibitors.

Explored in photodynamic therapy research for its ability to generate reactive oxygen species under light exposure.

Incorporated into dye-sensitized solar cells as a sensitizer to improve light absorption and energy conversion efficiency.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...