5-(4-Methoxyphenyl)-2H-tetrazole

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Reagent Code: #210138
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CAS Number 6926-51-8

science Other reagents with same CAS 6926-51-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 176.18 g/mol
Formula C₈H₈N₄O
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MDL Number MFCD00991875
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of angiotensin II receptor antagonists, particularly in the production of antihypertensive drugs like losartan and candesartan. Its tetrazole ring serves as a bioisostere for the carboxylic acid group, enhancing metabolic stability and improving pharmacokinetic properties. Also employed in coordination chemistry as a ligand for metal ions in catalytic systems. Shows potential in the development of new pharmaceuticals due to its ability to participate in hydrogen bonding and dipole interactions with biological targets.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,770.00
inventory 250mg
10-20 days ฿3,560.00
inventory 1g
10-20 days ฿5,560.50
inventory 5g
10-20 days ฿35,400.00

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5-(4-Methoxyphenyl)-2H-tetrazole
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Used as a key intermediate in the synthesis of angiotensin II receptor antagonists, particularly in the production of antihypertensive drugs like losartan and candesartan. Its tetrazole ring serves as a bioisostere for the carboxylic acid group, enhancing metabolic stability and improving pharmacokinetic properties. Also employed in coordination chemistry as a ligand for metal ions in catalytic systems. Shows potential in the development of new pharmaceuticals due to its ability to participate in hydrogen b
Used as a key intermediate in the synthesis of angiotensin II receptor antagonists, particularly in the production of antihypertensive drugs like losartan and candesartan. Its tetrazole ring serves as a bioisostere for the carboxylic acid group, enhancing metabolic stability and improving pharmacokinetic properties. Also employed in coordination chemistry as a ligand for metal ions in catalytic systems. Shows potential in the development of new pharmaceuticals due to its ability to participate in hydrogen bonding and dipole interactions with biological targets.
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