1-(2-chloropyridin-4-yl)hydrazine

≥95%

Reagent Code: #159315
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CAS Number 700811-29-6

science Other reagents with same CAS 700811-29-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 143.57 g/mol
Formula C₅H₆ClN₃
badge Registry Numbers
MDL Number MFCD08460247
thermostat Physical Properties
Melting Point 85-86 °C
Boiling Point 308.6±27.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.418±0.06 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the preparation of pyridine-based derivatives with biological activity. It serves as a building block for heterocyclic compounds that exhibit insecticidal, herbicidal, or fungicidal properties. Its hydrazine functionality allows for facile ring formation or coupling reactions, making it valuable in the development of novel active ingredients in crop protection agents. Also explored in medicinal chemistry for potential antimicrobial or antiviral applications due to the chloropyridine scaffold’s affinity for biological targets.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿760.00
1g
10-20 days ฿2,220.00
5g
10-20 days ฿10,370.00
1-(2-chloropyridin-4-yl)hydrazine
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Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the preparation of pyridine-based derivatives with biological activity. It serves as a building block for heterocyclic compounds that exhibit insecticidal, herbicidal, or fungicidal properties. Its hydrazine functionality allows for facile ring formation or coupling reactions, making it valuable in the development of novel active ingredients in crop protection agents. Also explored in medicinal chemistry for po

Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the preparation of pyridine-based derivatives with biological activity. It serves as a building block for heterocyclic compounds that exhibit insecticidal, herbicidal, or fungicidal properties. Its hydrazine functionality allows for facile ring formation or coupling reactions, making it valuable in the development of novel active ingredients in crop protection agents. Also explored in medicinal chemistry for potential antimicrobial or antiviral applications due to the chloropyridine scaffold’s affinity for biological targets.

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