4-(1H-Tetrazol-5-yl)benzaldehyde

≥95%

Reagent Code: #173761
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CAS Number 74815-22-8

science Other reagents with same CAS 74815-22-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 174.16 g/mol
Formula C₈H₆N₄O
badge Registry Numbers
MDL Number MFCD01311033
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of angiotensin II receptor antagonists, such as valsartan and other sartan-class antihypertensive drugs. Its tetrazole ring mimics the carboxylic acid group in biological systems, enhancing binding to the AT1 receptor. Also employed in coordination chemistry to form metal-organic frameworks due to its ability to act as a multidentate ligand. Additionally, it serves as a building block in click chemistry and pharmaceutical research for developing bioactive molecules.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿1,450.00
inventory 1g
10-20 days ฿5,400.00
inventory 5g
10-20 days ฿26,800.00

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4-(1H-Tetrazol-5-yl)benzaldehyde
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Used as a key intermediate in the synthesis of angiotensin II receptor antagonists, such as valsartan and other sartan-class antihypertensive drugs. Its tetrazole ring mimics the carboxylic acid group in biological systems, enhancing binding to the AT1 receptor. Also employed in coordination chemistry to form metal-organic frameworks due to its ability to act as a multidentate ligand. Additionally, it serves as a building block in click chemistry and pharmaceutical research for developing bioactive molec

Used as a key intermediate in the synthesis of angiotensin II receptor antagonists, such as valsartan and other sartan-class antihypertensive drugs. Its tetrazole ring mimics the carboxylic acid group in biological systems, enhancing binding to the AT1 receptor. Also employed in coordination chemistry to form metal-organic frameworks due to its ability to act as a multidentate ligand. Additionally, it serves as a building block in click chemistry and pharmaceutical research for developing bioactive molecules.

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