(2-Phenoxybenzyl)hydrazine hydrochloride

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Reagent Code: #227814
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CAS Number 2682114-51-6

science Other reagents with same CAS 2682114-51-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 250.72 g/mol
Formula C₁₃H₁₅ClN₂O
badge Registry Numbers
MDL Number MFCD32706982
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, inert gas

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of certain antihypertensive and antiarrhythmic agents. It serves as a building block in organic reactions where hydrazine functionality is required for coupling or cyclization processes. Its phenoxy-benzyl structure allows for good aromatic reactivity, making it useful in the preparation of heterocyclic systems. Also employed in research settings for the design of novel bioactive molecules and in the optimization of drug candidates requiring hydrazine-based modifications.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,950.00
inventory 1g
10-20 days ฿7,960.00
inventory 5g
10-20 days ฿27,850.00
inventory 25g
10-20 days ฿102,610.00

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(2-Phenoxybenzyl)hydrazine hydrochloride
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Used primarily as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of certain antihypertensive and antiarrhythmic agents. It serves as a building block in organic reactions where hydrazine functionality is required for coupling or cyclization processes. Its phenoxy-benzyl structure allows for good aromatic reactivity, making it useful in the preparation of heterocyclic systems. Also employed in research settings for the design of novel bioactive molecules and

Used primarily as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of certain antihypertensive and antiarrhythmic agents. It serves as a building block in organic reactions where hydrazine functionality is required for coupling or cyclization processes. Its phenoxy-benzyl structure allows for good aromatic reactivity, making it useful in the preparation of heterocyclic systems. Also employed in research settings for the design of novel bioactive molecules and in the optimization of drug candidates requiring hydrazine-based modifications.

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