(3-Methoxybenzyl)hydrazine dihydrochloride

98%

Reagent Code: #212306
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CAS Number 849021-11-0

science Other reagents with same CAS 849021-11-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 225.116 g/mol
Formula C₈H₁₄Cl₂N₂O
badge Registry Numbers
MDL Number MFCD06245507
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of selective kinase inhibitors and central nervous system agents. Its hydrazine functionality allows for coupling reactions with carbonyl compounds, enabling the formation of hydrazones that serve as building blocks in drug design. Commonly employed in medicinal chemistry for constructing heterocyclic scaffolds such as pyrazoles and triazoles. Also utilized in the preparation of serotonin receptor modulators and antidepressant candidates due to the presence of the methoxybenzyl moiety, which can enhance blood-brain barrier penetration. Shows utility in research settings for labeling and conjugation strategies in biochemical assays.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿970.00
inventory 1g
10-20 days ฿2,400.00
inventory 5g
10-20 days ฿8,960.00
inventory 25g
10-20 days ฿28,930.00

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(3-Methoxybenzyl)hydrazine dihydrochloride
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Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of selective kinase inhibitors and central nervous system agents. Its hydrazine functionality allows for coupling reactions with carbonyl compounds, enabling the formation of hydrazones that serve as building blocks in drug design. Commonly employed in medicinal chemistry for constructing heterocyclic scaffolds such as pyrazoles and triazoles. Also utilized in the preparation of serotonin receptor modulators and antidepressant candidates due to the presence of the methoxybenzyl moiety, which can enhance blood-brain barrier penetration. Shows utility in research settings for labeling and conjugation strategies in biochemical assays.
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