2,3-Dioxo-1,2,3,4-tetrahydroquinoxaline-6-sulfonyl chloride

98%

Reagent Code: #178829
fingerprint
CAS Number 952-10-3

science Other reagents with same CAS 952-10-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 260.65 g/mol
Formula C₈H₅ClN₂O₄S
badge Registry Numbers
MDL Number MFCD13187318
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals and agrochemicals. Its sulfonyl chloride group allows for easy attachment to amines or alcohols, forming sulfonamides or sulfonate esters, which are common motifs in drug design. It is also employed in the development of kinase inhibitors and other enzyme modulators due to the quinoxaline core’s affinity for binding biological targets. Additionally, it serves as a building block in the preparation of fluorescent dyes and sensors, where the conjugated structure contributes to light absorption and emission properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,450.00
inventory 250mg
10-20 days ฿2,120.00
inventory 5g
10-20 days ฿22,640.00
inventory 1g
10-20 days ฿7,240.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2,3-Dioxo-1,2,3,4-tetrahydroquinoxaline-6-sulfonyl chloride
No image available

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals and agrochemicals. Its sulfonyl chloride group allows for easy attachment to amines or alcohols, forming sulfonamides or sulfonate esters, which are common motifs in drug design. It is also employed in the development of kinase inhibitors and other enzyme modulators due to the quinoxaline core’s affinity for binding biological targets. Additionally, it serves as a building block in the preparation o

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals and agrochemicals. Its sulfonyl chloride group allows for easy attachment to amines or alcohols, forming sulfonamides or sulfonate esters, which are common motifs in drug design. It is also employed in the development of kinase inhibitors and other enzyme modulators due to the quinoxaline core’s affinity for binding biological targets. Additionally, it serves as a building block in the preparation of fluorescent dyes and sensors, where the conjugated structure contributes to light absorption and emission properties.

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...