2,5-Dichloro-3,4-dinitrothiophene

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Reagent Code: #179919
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CAS Number 51584-21-5

science Other reagents with same CAS 51584-21-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 243.03 g/mol
Formula C₄Cl₂N₂O₄S
badge Registry Numbers
MDL Number MFCD00052395
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals, this compound plays a key role in constructing complex heterocyclic systems. Its reactive chlorine and nitro groups allow for selective substitutions, making it valuable in the development of active ingredients in crop protection agents. It is also employed in research settings to build functionalized thiophene derivatives for materials science, including organic semiconductors and dyes. Due to its electron-deficient nature, it serves as a building block in cross-coupling reactions and nucleophilic aromatic substitution processes. Handling requires caution due to its potential sensitivity and reactivity.

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inventory 100mg
10-20 days ฿1,340.00

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2,5-Dichloro-3,4-dinitrothiophene
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Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals, this compound plays a key role in constructing complex heterocyclic systems. Its reactive chlorine and nitro groups allow for selective substitutions, making it valuable in the development of active ingredients in crop protection agents. It is also employed in research settings to build functionalized thiophene derivatives for materials science, including organic semiconductors and dyes. Due to its electron-deficient

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals, this compound plays a key role in constructing complex heterocyclic systems. Its reactive chlorine and nitro groups allow for selective substitutions, making it valuable in the development of active ingredients in crop protection agents. It is also employed in research settings to build functionalized thiophene derivatives for materials science, including organic semiconductors and dyes. Due to its electron-deficient nature, it serves as a building block in cross-coupling reactions and nucleophilic aromatic substitution processes. Handling requires caution due to its potential sensitivity and reactivity.

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