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Atomfair 2-Methyl-4-nitrobutan-1-ol C5H11NO3
Description 2-Methyl-4-nitrobutan-1-ol (CAS No. 1022985-41-6) is a high-purity nitro-alcohol compound with the molecular formula C5H11NO3. This specialized chemical is ideal for research and industrial applications requiring precise nitro-functionalized intermediates. Its IUPAC name, 2-methyl-4-nitrobutan-1-ol , reflects its branched alkyl chain with both hydroxyl and nitro moieties, offering unique reactivity for synthetic organic chemistry. Available in various quantities with guaranteed purity levels, this product is rigorously tested via GC/MS, NMR, and HPLC to ensure consistency. Suitable for use in pharmaceutical synthesis, material science, and agrochemical development. Store in a cool, dry place under inert conditions to maintain stability.
Description
Description
2-Methyl-4-nitrobutan-1-ol (CAS No. 1022985-41-6) is a high-purity nitro-alcohol compound with the molecular formula C5H11NO3. This specialized chemical is ideal for research and industrial applications requiring precise nitro-functionalized intermediates. Its IUPAC name, 2-methyl-4-nitrobutan-1-ol, reflects its branched alkyl chain with both hydroxyl and nitro moieties, offering unique reactivity for synthetic organic chemistry. Available in various quantities with guaranteed purity levels, this product is rigorously tested via GC/MS, NMR, and HPLC to ensure consistency. Suitable for use in pharmaceutical synthesis, material science, and agrochemical development. Store in a cool, dry place under inert conditions to maintain stability.
- CAS No: 1022985-41-6
- Molecular Formula: C5H11NO3
- Molecular Weight: 133.15
- Exact Mass: 133.07389321
- Monoisotopic Mass: 133.07389321
- IUPAC Name: 2-methyl-4-nitrobutan-1-ol
- SMILES: CC(CC[N+](=O)[O-])CO
- Synonyms: 2-methyl-4-nitrobutan-1-ol, SCHEMBL3328096, AKOS015841775, DB-058792, EN300-6506355
Application
2-Methyl-4-nitrobutan-1-ol serves as a versatile building block in organic synthesis, particularly for the preparation of nitroalkane derivatives. Researchers utilize it in pharmaceutical intermediate synthesis due to its reactive nitro and hydroxyl functional groups. It may also be employed in polymer chemistry as a modifier or crosslinking agent. Additionally, its structural properties make it a candidate for studying energetic materials or propellant formulations.
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