5-(2-Amino-4-chloro-5-sulfamoylphenyl)-1H-tetrazole

98%

Reagent Code: #136402
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CAS Number 82212-14-4

science Other reagents with same CAS 82212-14-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 274.68 g/mol
Formula C₇H₇ClN₆O₂S
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used in the synthesis of carbonic anhydrase inhibitors, particularly in the development of sulfonamide-based pharmaceuticals for treating glaucoma and certain types of epilepsy. Its tetrazole ring acts as a bioisostere for carboxylic acid, enhancing metabolic stability and improving membrane permeability in drug candidates. Also employed in medicinal chemistry research to design novel heterocyclic compounds with potential diuretic and anticonvulsant activities.

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Test Parameter Specification
Appearance White to Beige to Light red to Green powder to crystalline
Purity (%) 97.5-100
NMR SPECTRUM 1H Conforms to Structure
LC-MS for identification Conforms

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿3,320.00
5-(2-Amino-4-chloro-5-sulfamoylphenyl)-1H-tetrazole
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Used in the synthesis of carbonic anhydrase inhibitors, particularly in the development of sulfonamide-based pharmaceuticals for treating glaucoma and certain types of epilepsy. Its tetrazole ring acts as a bioisostere for carboxylic acid, enhancing metabolic stability and improving membrane permeability in drug candidates. Also employed in medicinal chemistry research to design novel heterocyclic compounds with potential diuretic and anticonvulsant activities.

Used in the synthesis of carbonic anhydrase inhibitors, particularly in the development of sulfonamide-based pharmaceuticals for treating glaucoma and certain types of epilepsy. Its tetrazole ring acts as a bioisostere for carboxylic acid, enhancing metabolic stability and improving membrane permeability in drug candidates. Also employed in medicinal chemistry research to design novel heterocyclic compounds with potential diuretic and anticonvulsant activities.

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