2-(4-Nitro-1H-pyrazol-1-yl)ethanol

≥95%

Reagent Code: #218156
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CAS Number 42027-81-6

science Other reagents with same CAS 42027-81-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 157.13 g/mol
Formula C₅H₇N₃O₃
badge Registry Numbers
MDL Number MFCD06740528
thermostat Physical Properties
Boiling Point 343.5°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry seal

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its structure allows for functionalization at multiple sites, making it valuable in the development of bioactive molecules. Commonly employed in the synthesis of pyrazole-containing compounds, which exhibit a range of biological activities including anti-inflammatory, antimicrobial, and antitumor properties. Also utilized in the design of novel heterocyclic compounds for medicinal chemistry research. The hydroxyl and nitro groups enable further chemical modifications, such as reduction of the nitro group to an amine for use in coupling reactions or conversion of the alcohol to esters and ethers to fine-tune solubility and reactivity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,480.00
inventory 1g
10-20 days ฿7,370.00
inventory 5g
10-20 days ฿21,020.00
inventory 10g
10-20 days ฿37,110.00

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2-(4-Nitro-1H-pyrazol-1-yl)ethanol
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its structure allows for functionalization at multiple sites, making it valuable in the development of bioactive molecules. Commonly employed in the synthesis of pyrazole-containing compounds, which exhibit a range of biological activities including anti-inflammatory, antimicrobial, and antitumor properties. Also utilized in the design of novel heterocyclic compounds for medicinal chemistry

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its structure allows for functionalization at multiple sites, making it valuable in the development of bioactive molecules. Commonly employed in the synthesis of pyrazole-containing compounds, which exhibit a range of biological activities including anti-inflammatory, antimicrobial, and antitumor properties. Also utilized in the design of novel heterocyclic compounds for medicinal chemistry research. The hydroxyl and nitro groups enable further chemical modifications, such as reduction of the nitro group to an amine for use in coupling reactions or conversion of the alcohol to esters and ethers to fine-tune solubility and reactivity.

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