Ethyl 3-(chlorosulfonyl)isonicotinate

98%

Reagent Code: #184803
label
Alias Ethyl 3-Chlorosulfonic acid isonic acid
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CAS Number 306936-12-9

science Other reagents with same CAS 306936-12-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 249.67 g/mol
Formula C₈H₈ClNO₄S
badge Registry Numbers
MDL Number MFCD01313855
thermostat Physical Properties
Boiling Point 376.7±27.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of sulfonamide-based drugs. Its reactive chlorosulfonyl group allows for easy attachment to amines, forming sulfonamide linkages common in antimicrobial and anti-inflammatory agents. Also employed in agrochemical synthesis for creating herbicides and plant growth regulators. Its ester functionality enables further modification, making it valuable in organic synthesis for building complex heterocyclic compounds.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,940.00
inventory 250mg
10-20 days ฿3,280.00
inventory 1g
10-20 days ฿11,560.00

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Ethyl 3-(chlorosulfonyl)isonicotinate
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of sulfonamide-based drugs. Its reactive chlorosulfonyl group allows for easy attachment to amines, forming sulfonamide linkages common in antimicrobial and anti-inflammatory agents. Also employed in agrochemical synthesis for creating herbicides and plant growth regulators. Its ester functionality enables further modification, making it valuable in organic synthesis for building complex heterocyclic compounds.

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of sulfonamide-based drugs. Its reactive chlorosulfonyl group allows for easy attachment to amines, forming sulfonamide linkages common in antimicrobial and anti-inflammatory agents. Also employed in agrochemical synthesis for creating herbicides and plant growth regulators. Its ester functionality enables further modification, making it valuable in organic synthesis for building complex heterocyclic compounds.

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