2-phenylethene-1-sulfonyl chloride

2-phenylethene-1-sulfonyl chloride

2-(2-methoxy-4-(trifluoromethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

2-(2-methoxy-4-(trifluoromethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

(3,4,5-tris(octadecyloxy)phenyl)methanol

$300.00
CAS No.: 233281-31-7
Catalog No.: 197486
Purity: 95%
MF: C61H116O4
MW: 913.595
Storage: 2-8 degree Celsius
SMILES: C(CCCCCCCCCCCCCCCCC)OC=1C=C(C=C(C1OCCCCCCCCCCCCCCCCCC)OCCCCCCCCCCCCCCCCCC)CO
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197486
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(3,4,5-tris(octadecyloxy)phenyl)methanol; CAS No.: 233281-31-7; (3,4,5-tris(octadecyloxy)phenyl)methanol. PROPERTIES: This tris(octadecyloxy)-substituted phenylmethanol features molecular formula C??H???O? with molecular weight 883.45 g/mol. It generally appears as a white crystalline powder. Soluble in non-polar and slightly polar organic solvents like hexanes and ethyl acetate. Melting point approximately 70-75 C. Exhibits IR absorption for hydroxyl groups (~3300 cm??) and ether (~1200-1000 cm??). Thermogravimetric analysis reveals weight loss onset above 180 C under nitrogen. For optimal stability, store at 2-8 C in tightly sealed containers with desiccant, protected from light. The compound may cause severe skin burns and eye damage; therefore, rigorous containment and personal protection measures are essential during manipulation. APPLICATIONS: As a tris(octadecyloxy)-substituted phenylmethanol, (3,4,5-tris(octadecyloxy)phenyl)methanol is predominantly utilized in the synthesis of liquid crystal materials. It serves as a key intermediate in constructing mesogenic units for liquid crystal displays, where the long alkyl chains provide valuable phase transition properties as demonstrated in materials science research (Liquid Crystals). Additionally, the compound participates in the development of surfactants and detergents, where its hydroxyl group enhances solubility and surface activity (Langmuir). In medicinal chemistry, it functions as a building block for constructing lipophilic drug delivery systems, where the octadecyloxy substituents enhance membrane penetration (Journal of Medicinal Chemistry).

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