3-(4-Chlorophenylsulfonamido)propanoic acid

98%

Reagent Code: #163269
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CAS Number 36974-65-9

science Other reagents with same CAS 36974-65-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 263.70 g/mol
Formula C₉H₁₀ClNO₄S
badge Registry Numbers
MDL Number MFCD00455382
thermostat Physical Properties
Melting Point 145-153 °C
Boiling Point 459.6 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.468±0.06 g/cm3(Predicted)
Storage Room temperature, sealed, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of sulfonamide-based drugs with potential antimicrobial and anti-inflammatory properties. It serves as a building block for modifying molecular structures to enhance drug efficacy and selectivity. Also employed in research settings for designing enzyme inhibitors due to the sulfonamide group's ability to interact with biological targets. Its carboxylic acid functionality allows for further chemical derivatization, making it valuable in medicinal chemistry and drug discovery processes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,860.00
inventory 250mg
10-20 days ฿4,270.00
inventory 1g
10-20 days ฿13,040.00

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3-(4-Chlorophenylsulfonamido)propanoic acid
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of sulfonamide-based drugs with potential antimicrobial and anti-inflammatory properties. It serves as a building block for modifying molecular structures to enhance drug efficacy and selectivity. Also employed in research settings for designing enzyme inhibitors due to the sulfonamide group's ability to interact with biological targets. Its carboxylic acid functionality allows for further chemical deriv

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of sulfonamide-based drugs with potential antimicrobial and anti-inflammatory properties. It serves as a building block for modifying molecular structures to enhance drug efficacy and selectivity. Also employed in research settings for designing enzyme inhibitors due to the sulfonamide group's ability to interact with biological targets. Its carboxylic acid functionality allows for further chemical derivatization, making it valuable in medicinal chemistry and drug discovery processes.

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