3-Nitrobenzothioamide

95%

Reagent Code: #219242
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CAS Number 70102-34-0

science Other reagents with same CAS 70102-34-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 182.20 g/mol
Formula C₇H₆N₂O₂S
badge Registry Numbers
MDL Number MFCD09757586
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with antimicrobial and antifungal properties. It serves as a building block in heterocyclic chemistry, facilitating the formation of thiazole and thiadiazole derivatives. Also employed in the preparation of dyes and pigments due to its aromatic and sulfur-containing structure. Its nitro group allows for further functionalization through reduction to amino derivatives, enabling diverse chemical transformations in research and industrial applications.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿940.00
250mg
10-20 days ฿1,640.00
1g
10-20 days ฿3,240.00
5g
10-20 days ฿10,400.00
3-Nitrobenzothioamide
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with antimicrobial and antifungal properties. It serves as a building block in heterocyclic chemistry, facilitating the formation of thiazole and thiadiazole derivatives. Also employed in the preparation of dyes and pigments due to its aromatic and sulfur-containing structure. Its nitro group allows for further functionalization through reduction to amino derivatives, enab

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with antimicrobial and antifungal properties. It serves as a building block in heterocyclic chemistry, facilitating the formation of thiazole and thiadiazole derivatives. Also employed in the preparation of dyes and pigments due to its aromatic and sulfur-containing structure. Its nitro group allows for further functionalization through reduction to amino derivatives, enabling diverse chemical transformations in research and industrial applications.

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