3-Amino-4-pyrazolecarboxamide hemisulfate salt

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Reagent Code: #134590
label
Alias 3-amino-4-formaminopyrazole hemisulfate; 3-aminopyrazole-4-formamide sulfate, 3-aminopyridine-4-formamide hemisulfate
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CAS Number 27511-79-1

science Other reagents with same CAS 27511-79-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 175.16 g/mol
Formula C₄H₆N₄O·₁/₂H₂SO₄
badge Registry Numbers
EC Number 248-503-6
MDL Number MFCD00013093
thermostat Physical Properties
Melting Point 224 °C (dec.)(lit.)
inventory_2 Storage & Handling
Density 0.84
Storage Room temperature

description Product Description

Used in pharmaceutical synthesis as a key intermediate for nitrogen-containing heterocyclic compounds, particularly in the development of kinase inhibitors and anti-inflammatory agents. Its structure supports cyclization reactions that form bioactive pyrazole derivatives. Also employed in agrochemical research for designing novel pesticides with improved selectivity. The hemisulfate salt form enhances solubility and stability during reaction processes, making it suitable for aqueous-phase synthesis. Additionally, explored in materials science for constructing functionalized polymers with thermal stability.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿138.00
inventory 5g
10-20 days ฿148.50
inventory 25g
10-20 days ฿440.00
inventory 100g
10-20 days ฿1,220.00
inventory 500g
10-20 days ฿5,360.00
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3-Amino-4-pyrazolecarboxamide hemisulfate salt
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Used in pharmaceutical synthesis as a key intermediate for nitrogen-containing heterocyclic compounds, particularly in the development of kinase inhibitors and anti-inflammatory agents. Its structure supports cyclization reactions that form bioactive pyrazole derivatives. Also employed in agrochemical research for designing novel pesticides with improved selectivity. The hemisulfate salt form enhances solubility and stability during reaction processes, making it suitable for aqueous-phase synthesis. Addi

Used in pharmaceutical synthesis as a key intermediate for nitrogen-containing heterocyclic compounds, particularly in the development of kinase inhibitors and anti-inflammatory agents. Its structure supports cyclization reactions that form bioactive pyrazole derivatives. Also employed in agrochemical research for designing novel pesticides with improved selectivity. The hemisulfate salt form enhances solubility and stability during reaction processes, making it suitable for aqueous-phase synthesis. Additionally, explored in materials science for constructing functionalized polymers with thermal stability.

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