4-(2H-Tetrazol-5-yl)aniline

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Reagent Code: #196354
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CAS Number 46047-18-1

science Other reagents with same CAS 46047-18-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 161.16 g/mol
Formula C₇H₇N₅
badge Registry Numbers
MDL Number MFCD06738320
thermostat Physical Properties
Melting Point 265 °C
Boiling Point 418.8±47.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.401±0.06 g/cm3(Predicted)
Storage 2-8°C, storage away from light, inert atmosphere

description Product Description

Used as a key intermediate in the synthesis of angiotensin II receptor antagonists, such as losartan and valsartan, which are widely prescribed for the treatment of hypertension and heart failure. Its tetrazole ring mimics the carboxylic acid group in biological systems, enhancing binding affinity to the receptor. Also employed in the development of other pharmaceuticals and agrochemicals due to its ability to participate in coordination and hydrogen bonding. Additionally, finds use in materials science for constructing nitrogen-rich polymers and ligands in catalysis.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿980.00
inventory 250mg
10-20 days ฿1,950.00
inventory 1g
10-20 days ฿4,500.00
inventory 5g
10-20 days ฿14,270.00
inventory 25g
10-20 days ฿46,020.00

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4-(2H-Tetrazol-5-yl)aniline
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Used as a key intermediate in the synthesis of angiotensin II receptor antagonists, such as losartan and valsartan, which are widely prescribed for the treatment of hypertension and heart failure. Its tetrazole ring mimics the carboxylic acid group in biological systems, enhancing binding affinity to the receptor. Also employed in the development of other pharmaceuticals and agrochemicals due to its ability to participate in coordination and hydrogen bonding. Additionally, finds use in materials science

Used as a key intermediate in the synthesis of angiotensin II receptor antagonists, such as losartan and valsartan, which are widely prescribed for the treatment of hypertension and heart failure. Its tetrazole ring mimics the carboxylic acid group in biological systems, enhancing binding affinity to the receptor. Also employed in the development of other pharmaceuticals and agrochemicals due to its ability to participate in coordination and hydrogen bonding. Additionally, finds use in materials science for constructing nitrogen-rich polymers and ligands in catalysis.

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