(4-((1H-Tetrazol-5-yl)carbamoyl)phenyl)boronic acid hydrochloride

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Reagent Code: #197080
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CAS Number 850568-31-9

science Other reagents with same CAS 850568-31-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 269.45 g/mol
Formula C₈H₈BN₅O₃^.HCl
badge Registry Numbers
MDL Number MFCD06659882
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of angiotensin II receptor antagonists for treating hypertension. Acts as a key building block in Suzuki-Miyaura cross-coupling reactions, enabling the formation of biaryl structures found in active drug molecules. Its tetrazole and boronic acid functional groups provide dual reactivity, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Also employed in the preparation of protease inhibitors and in research related to glucose-sensing materials due to boronic acid’s affinity for diols.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,130.00
inventory 1g
10-20 days ฿11,120.00
inventory 5g
10-20 days ฿42,150.00

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(4-((1H-Tetrazol-5-yl)carbamoyl)phenyl)boronic acid hydrochloride
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Used in the synthesis of pharmaceutical intermediates, particularly in the development of angiotensin II receptor antagonists for treating hypertension. Acts as a key building block in Suzuki-Miyaura cross-coupling reactions, enabling the formation of biaryl structures found in active drug molecules. Its tetrazole and boronic acid functional groups provide dual reactivity, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Also employed in the preparation of protease

Used in the synthesis of pharmaceutical intermediates, particularly in the development of angiotensin II receptor antagonists for treating hypertension. Acts as a key building block in Suzuki-Miyaura cross-coupling reactions, enabling the formation of biaryl structures found in active drug molecules. Its tetrazole and boronic acid functional groups provide dual reactivity, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Also employed in the preparation of protease inhibitors and in research related to glucose-sensing materials due to boronic acid’s affinity for diols.

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