1-Benzenesulfonyl-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid

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Reagent Code: #148691
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CAS Number 189089-90-5

science Other reagents with same CAS 189089-90-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 302.31 g/mol
Formula C₁₄H₁₀N₂O₄S
badge Registry Numbers
MDL Number MFCD02083337
thermostat Physical Properties
Boiling Point 587.064°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry seal

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to enzyme active sites, making it valuable in drug discovery for targeted therapies. Also utilized in research settings to design compounds with anti-inflammatory and antiviral properties. The compound's sulfonyl and carboxylic functional groups allow for diverse chemical modifications, enhancing its utility in creating libraries of bioactive molecules.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿5,050.00
inventory 5g
10-20 days ฿18,350.00
inventory 250mg
10-20 days ฿2,020.00

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1-Benzenesulfonyl-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to enzyme active sites, making it valuable in drug discovery for targeted therapies. Also utilized in research settings to design compounds with anti-inflammatory and antiviral properties. The compound's sulfonyl and carboxylic functional groups allow for diverse chemical modifications, enhancing its utility in creating libraries o

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to enzyme active sites, making it valuable in drug discovery for targeted therapies. Also utilized in research settings to design compounds with anti-inflammatory and antiviral properties. The compound's sulfonyl and carboxylic functional groups allow for diverse chemical modifications, enhancing its utility in creating libraries of bioactive molecules.

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