5-(2-Iodophenyl)-1H-tetrazole

98%(T)

Reagent Code: #199957
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CAS Number 73096-40-9

science Other reagents with same CAS 73096-40-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 272.05 g/mol
Formula C₇H₅IN₄
badge Registry Numbers
MDL Number MFCD07779116
thermostat Physical Properties
Melting Point 214°C(分解)
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of angiotensin II receptor antagonists, particularly in the production of sartan-class antihypertensive drugs such as losartan and valsartan. Its structure enables effective coupling in medicinal chemistry pathways, making it valuable for developing pharmaceuticals that regulate blood pressure. Also employed in research for designing novel bioactive molecules due to the tetrazole ring’s ability to mimic carboxylic acid groups, enhancing metabolic stability and bioavailability in drug candidates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿170.50
inventory 250mg
10-20 days ฿242.00
inventory 1g
10-20 days ฿676.50
inventory 5g
10-20 days ฿2,266.00

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5-(2-Iodophenyl)-1H-tetrazole
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Used as a key intermediate in the synthesis of angiotensin II receptor antagonists, particularly in the production of sartan-class antihypertensive drugs such as losartan and valsartan. Its structure enables effective coupling in medicinal chemistry pathways, making it valuable for developing pharmaceuticals that regulate blood pressure. Also employed in research for designing novel bioactive molecules due to the tetrazole ring’s ability to mimic carboxylic acid groups, enhancing metabolic stability and

Used as a key intermediate in the synthesis of angiotensin II receptor antagonists, particularly in the production of sartan-class antihypertensive drugs such as losartan and valsartan. Its structure enables effective coupling in medicinal chemistry pathways, making it valuable for developing pharmaceuticals that regulate blood pressure. Also employed in research for designing novel bioactive molecules due to the tetrazole ring’s ability to mimic carboxylic acid groups, enhancing metabolic stability and bioavailability in drug candidates.

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