4-bromo-7-methyl-2,1,3-benzothiadiazole

98%

Reagent Code: #146903
fingerprint
CAS Number 2255-80-3

science Other reagents with same CAS 2255-80-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 229.09 g/mol
Formula C₇H₅BrN₂S
thermostat Physical Properties
Boiling Point 292.746°C
inventory_2 Storage & Handling
Density 1.736 g/mL
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of fluorescent dyes and optoelectronic materials due to its strong electron-accepting properties and ability to form conjugated systems. Commonly employed in the development of organic semiconductors, sensors, and luminescent probes for biological imaging. Its bromine functionality allows for easy functionalization via cross-coupling reactions, making it valuable in medicinal chemistry for building complex heterocyclic compounds. Also applied in the preparation of fluorescent tags for detecting biomolecules and in the design of solar cell materials.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿890.00
inventory 250mg
10-20 days ฿2,090.00
inventory 1g
10-20 days ฿5,580.00
inventory 5g
10-20 days ฿22,680.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
4-bromo-7-methyl-2,1,3-benzothiadiazole
No image available
Used as a key intermediate in the synthesis of fluorescent dyes and optoelectronic materials due to its strong electron-accepting properties and ability to form conjugated systems. Commonly employed in the development of organic semiconductors, sensors, and luminescent probes for biological imaging. Its bromine functionality allows for easy functionalization via cross-coupling reactions, making it valuable in medicinal chemistry for building complex heterocyclic compounds. Also applied in the preparation of
Used as a key intermediate in the synthesis of fluorescent dyes and optoelectronic materials due to its strong electron-accepting properties and ability to form conjugated systems. Commonly employed in the development of organic semiconductors, sensors, and luminescent probes for biological imaging. Its bromine functionality allows for easy functionalization via cross-coupling reactions, making it valuable in medicinal chemistry for building complex heterocyclic compounds. Also applied in the preparation of fluorescent tags for detecting biomolecules and in the design of solar cell materials.
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...