6-Nitro-1H-indole-3-sulfonyl chloride

95%

Reagent Code: #219531
fingerprint
CAS Number 132745-00-7

science Other reagents with same CAS 132745-00-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 260.65 g/mol
Formula C₈H₅ClN₂O₄S
badge Registry Numbers
MDL Number MFCD00451765
inventory_2 Storage & Handling
Storage 2-8°C, avoiding light

description Product Description

Used as a key intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals. Its structure allows for functionalization at multiple sites, making it valuable in creating indole-based drug candidates. Commonly employed in the preparation of sulfonamide derivatives, which are explored for their antimicrobial, anti-inflammatory, and anticancer properties. Also utilized in agrochemical research for designing new pesticides and herbicides due to its electron-withdrawing nitro group and reactive sulfonyl chloride functionality.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿790.00
inventory 250mg
10-20 days ฿1,150.00
inventory 1g
10-20 days ฿4,420.00
inventory 5g
10-20 days ฿19,510.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
6-Nitro-1H-indole-3-sulfonyl chloride
No image available

Used as a key intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals. Its structure allows for functionalization at multiple sites, making it valuable in creating indole-based drug candidates. Commonly employed in the preparation of sulfonamide derivatives, which are explored for their antimicrobial, anti-inflammatory, and anticancer properties. Also utilized in agrochemical research for designing new pesticides and herbicides due to its electro

Used as a key intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals. Its structure allows for functionalization at multiple sites, making it valuable in creating indole-based drug candidates. Commonly employed in the preparation of sulfonamide derivatives, which are explored for their antimicrobial, anti-inflammatory, and anticancer properties. Also utilized in agrochemical research for designing new pesticides and herbicides due to its electron-withdrawing nitro group and reactive sulfonyl chloride functionality.

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...