1-Phenyltetrazole-5-thiol

98%

Reagent Code: #225050
label
Alias 1-phenyl-1H-tetrazol-5-thiol; 1-phenyltetrazol-5-thiol; 1-phenyl-5-mercapto-1H-1,2,3,4-tetrazol; 1-phenyl-5-thioltetrazol
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CAS Number 86-93-1

science Other reagents with same CAS 86-93-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 178.21 g/mol
Formula C₇H₆N₄S
badge Registry Numbers
MDL Number MFCD00003129
thermostat Physical Properties
Melting Point 145 °C(dec.)
inventory_2 Storage & Handling
Storage Room temperature, sealed

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 hypertension treatment. Its thiol and tetrazole groups enhance binding affinity to biological targets and improve metabolic stability. Also employed in coordination chemistry as a ligand for metal ions, forming complexes with potential catalytic or antimicrobial properties. Additionally, finds use in material science for developing heterocyclic polymers and corrosion inhibitors.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿300.00
inventory 25g
10-20 days ฿580.00
inventory 100g
10-20 days ฿2,180.00
inventory 500g
10-20 days ฿9,650.00
inventory 2.5kg
10-20 days ฿47,980.00

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1-Phenyltetrazole-5-thiol
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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 hypertension treatment. Its thiol and tetrazole groups enhance binding affinity to biological targets and improve metabolic stability. Also employed in coordination chemistry as a ligand for metal ions, forming complexes with potential catalytic or antimicrobial properties. Additionally, finds use in material science for developing heterocyclic polymers and c

Used as a key intermediate in the synthesis of angiotensin II receptor antagonists, such as losartan and valsartan, which are widely prescribed for hypertension treatment. Its thiol and tetrazole groups enhance binding affinity to biological targets and improve metabolic stability. Also employed in coordination chemistry as a ligand for metal ions, forming complexes with potential catalytic or antimicrobial properties. Additionally, finds use in material science for developing heterocyclic polymers and corrosion inhibitors.

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