Atomfair 4-(1-Hydroxypropyl)benzene-1,2-diol C9H12O3

Description 4-(1-Hydroxypropyl)benzene-1,2-diol (CAS No. 30766-03-1) is a high-purity catechol derivative with the molecular formula C9H12O3. This compound features a hydroxylated benzene ring substituted with a 1-hydroxypropyl group at the 4-position, making it a valuable intermediate in organic synthesis and pharmaceutical research. Its structural properties enable versatile reactivity, including electrophilic aromatic substitution and oxidation reactions. Ideal for researchers, this product is rigorously tested for purity and consistency, ensuring reliable performance in sensitive applications. Available in various quantities, it is supplied with comprehensive analytical data (including NMR, HPLC, and MS) to meet stringent laboratory standards.

Description

4-(1-Hydroxypropyl)benzene-1,2-diol (CAS No. 30766-03-1) is a high-purity catechol derivative with the molecular formula C₉H₁₂O₃. This compound features a hydroxylated benzene ring substituted with a 1-hydroxypropyl group at the 4-position, making it a valuable intermediate in organic synthesis and pharmaceutical research. Its structural properties enable versatile reactivity, including electrophilic aromatic substitution and oxidation reactions. Ideal for researchers, this product is rigorously tested for purity and consistency, ensuring reliable performance in sensitive applications. Available in various quantities, it is supplied with comprehensive analytical data (including NMR, HPLC, and MS) to meet stringent laboratory standards.

CAS No: 30766-03-1
Molecular Formula: C9H12O3
Molecular Weight: 168.19
Exact Mass: 168.078644241
Monoisotopic Mass: 168.078644241
IUPAC Name: 4-(1-hydroxypropyl)benzene-1,2-diol
SMILES: CCC(C1=CC(=C(C=C1)O)O)O
Synonyms: 25474-45-7, 4-(1-hydroxypropyl)benzene-1,2-diol, BRN 2965806, 4-(1-Hydroxypropyl)-1,2-benzenediol, 1,2-Benzenediol, 4-(1-hydroxypropyl)-

Application

4-(1-Hydroxypropyl)benzene-1,2-diol serves as a key building block in the synthesis of bioactive molecules, particularly in pharmaceutical and agrochemical research. Its catechol moiety is useful for developing antioxidants, enzyme inhibitors, and metal-chelating agents. Researchers also employ it in polymer chemistry to modify phenolic resins or as a precursor for functionalized aromatic compounds. Its reactivity makes it suitable for studying oxidative pathways in biochemical systems.

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