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Structure of 20274-69-5
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4-Fluoro-3-nitrobenzyl alcohol features a fluorinated benzyl scaffold with complementary nitro and hydroxyl functionalities, enabling selective derivatization in synthetic organic chemistry. The electron-deficient aromatic ring enhances reactivity in nucleophilic substitution cascades, while the primary alcohol facilitates coupling reactions under mild conditions. This compound serves as a versatile intermediate for bioactive molecule synthesis.
4-Fluoro-3-nitrobenzyl alcohol serves as a versatile building block in medicinal chemistry, enabling site-selective functionalization via the benzylic alcohol group. The ortho-fluoro and meta-nitro substituents provide complementary reactivity for cross-coupling and reduction strategies, while the alcohol facilitates derivatization or protection. Bench-stable and compatible with standard purification methods, it functions effectively in multi-step syntheses of heterocyclic scaffolds and bioactive molecules.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H319
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: