(R)-(1-(2,4-Dichlorophenyl)ethyl)hydrazine hydrochloride

95%

Reagent Code: #230724
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CAS Number 2174940-53-3

science Other reagents with same CAS 2174940-53-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 241.5 g/mol
Formula C₈H₁₁Cl₃N₂
inventory_2 Storage & Handling
Storage 2-8°C, dry, closed

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of antifungal agents such as voriconazole and other triazole-based drugs. Its chiral structure allows for selective biological activity, making it valuable in asymmetric synthesis. The compound is also employed in the development of agrochemicals and bioactive molecules where stereochemistry plays a critical role in efficacy. Its hydrazine functionality enables coupling reactions to form heterocyclic systems important in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿20,280.00
inventory 1g
10-20 days ฿50,710.00

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(R)-(1-(2,4-Dichlorophenyl)ethyl)hydrazine hydrochloride
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Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of antifungal agents such as voriconazole and other triazole-based drugs. Its chiral structure allows for selective biological activity, making it valuable in asymmetric synthesis. The compound is also employed in the development of agrochemicals and bioactive molecules where stereochemistry plays a critical role in efficacy. Its hydrazine functionality enables coupling reactions to form heterocyclic sys

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of antifungal agents such as voriconazole and other triazole-based drugs. Its chiral structure allows for selective biological activity, making it valuable in asymmetric synthesis. The compound is also employed in the development of agrochemicals and bioactive molecules where stereochemistry plays a critical role in efficacy. Its hydrazine functionality enables coupling reactions to form heterocyclic systems important in medicinal chemistry.

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