2-Amino-5-nitrothiazole

98%

Reagent Code: #135095
label
Alias 5-nitro-2-thiazolid; acetamide nithiazolid; amine nithiazolid; niamide nithiazolid; niamide thiazolid;
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CAS Number 121-66-4

science Other reagents with same CAS 121-66-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 145.14 g/mol
Formula C₃H₃N₃O₂S
badge Registry Numbers
EC Number 204-490-9
MDL Number MFCD00005326
thermostat Physical Properties
Melting Point 195-200 °C
Boiling Point 345.1ºC
inventory_2 Storage & Handling
Density 1.682g/cm3
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of sulfathiazole, a sulfonamide antibiotic. It also serves in the development of agrochemicals and dyes due to its reactive amino and nitro functional groups. Its structure supports the creation of biologically active compounds, making it valuable in medicinal chemistry research. Additionally, it is employed in the preparation of corrosion inhibitors and in some polymer stabilization processes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿300.00
inventory 100g
10-20 days ฿530.00
inventory 500g
10-20 days ฿2,450.00
inventory 2.5kg
10-20 days ฿12,020.00

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2-Amino-5-nitrothiazole
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of sulfathiazole, a sulfonamide antibiotic. It also serves in the development of agrochemicals and dyes due to its reactive amino and nitro functional groups. Its structure supports the creation of biologically active compounds, making it valuable in medicinal chemistry research. Additionally, it is employed in the preparation of corrosion inhibitors and in some polymer stabilization processes.

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of sulfathiazole, a sulfonamide antibiotic. It also serves in the development of agrochemicals and dyes due to its reactive amino and nitro functional groups. Its structure supports the creation of biologically active compounds, making it valuable in medicinal chemistry research. Additionally, it is employed in the preparation of corrosion inhibitors and in some polymer stabilization processes.

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