1-Acetylindoline-5-sulfonyl chloride

98%

Reagent Code: #137554
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CAS Number 52206-05-0

science Other reagents with same CAS 52206-05-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 257.69 g/mol
Formula C₁₀H₈ClNO₃S
badge Registry Numbers
MDL Number MFCD07368558
inventory_2 Storage & Handling
Storage 2-8°C, inert gas storage

description Product Description

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its sulfonyl chloride group readily reacts with amines to form sulfonamides, which are common motifs in drug design. It is also employed in the preparation of selective enzyme inhibitors and receptor modulators due to the stability and favorable pharmacokinetic properties imparted by the acetylindoline scaffold. Commonly utilized in medicinal chemistry research for building novel compounds with potential antidepressant, antipsychotic, or anti-inflammatory activity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿540.00
inventory 1g
10-20 days ฿1,400.00
inventory 5g
10-20 days ฿6,070.00
inventory 25g
10-20 days ฿26,700.00

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1-Acetylindoline-5-sulfonyl chloride
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Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its sulfonyl chloride group readily reacts with amines to form sulfonamides, which are common motifs in drug design. It is also employed in the preparation of selective enzyme inhibitors and receptor modulators due to the stability and favorable pharmacokinetic properties imparted by the acetylindoline scaffold. Commonly utilized in medicinal chemistry res

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its sulfonyl chloride group readily reacts with amines to form sulfonamides, which are common motifs in drug design. It is also employed in the preparation of selective enzyme inhibitors and receptor modulators due to the stability and favorable pharmacokinetic properties imparted by the acetylindoline scaffold. Commonly utilized in medicinal chemistry research for building novel compounds with potential antidepressant, antipsychotic, or anti-inflammatory activity.

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