6-Aminobenzo[b]thiophene 1,1-dioxide

97%

Reagent Code: #135839
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CAS Number 20503-40-6

science Other reagents with same CAS 20503-40-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 181.21 g/mol
Formula C₈H₇NO₂S
badge Registry Numbers
MDL Number MFCD00173800
thermostat Physical Properties
Melting Point 150°C
Boiling Point 467.4°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders and inflammation. Its structure supports the development of selective receptor modulators due to its ability to mimic aromatic amino acid motifs. Commonly employed in the preparation of sulfonamide-based drugs where enhanced metabolic stability and binding affinity are required. Also utilized in agrochemicals for designing herbicides and fungicides owing to its electron-deficient core and favorable solubility profile.

format_list_bulleted Product Specification

Test Parameter Specification
APPEARANCE Light yellow to yellow Solid
Purity (%) 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

Available Sizes & Pricing

Size Availability Unit Price Quantity
50mg
10-20 days ฿214.50
250mg
10-20 days ฿627.00
6-Aminobenzo[b]thiophene 1,1-dioxide
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Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders and inflammation. Its structure supports the development of selective receptor modulators due to its ability to mimic aromatic amino acid motifs. Commonly employed in the preparation of sulfonamide-based drugs where enhanced metabolic stability and binding affinity are required. Also utilized in agrochemicals for designing herbicides and fungicides owing

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders and inflammation. Its structure supports the development of selective receptor modulators due to its ability to mimic aromatic amino acid motifs. Commonly employed in the preparation of sulfonamide-based drugs where enhanced metabolic stability and binding affinity are required. Also utilized in agrochemicals for designing herbicides and fungicides owing to its electron-deficient core and favorable solubility profile.

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