122060-82-6

Basic information

• Product Name: Benzoyl chloride, 3,5-bis(decyloxy)-
• CAS NO: 122060-82-6
• Molecular Formula: C27H45ClO3
• Molecular Weight: 453.106
• Mol File: 122060-82-6.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Benzoyl chloride, 3,5-bis(decyloxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoyl chloride, 3,5-bis(decyloxy)-(122060-82-6)
• EPA Substance Registry System: Benzoyl chloride, 3,5-bis(decyloxy)-(122060-82-6)

Safety Data

• Hazardous Substances Data: 122060-82-6(Hazardous Substances Data)

Upstream product

• 125482-07-7 (3,5)-bis(decyloxy)benzoic acid 
• 125482-06-6 methyl 3,5-bis(decyloxy)benzoate 
• 2150-44-9 1-carbomethoxy-3,5-dihydroxybenzene 
• 112-29-8 1-bromo dodecane 

Downstream Products

• 1630946-09-6 C₇₄H₁₀₀N₂O₈S₂ 
• 1240520-28-8 3,5-di-(decyloxy)benzoic acid N-3,5-di-(decyloxy)benzoyl hydrazide 
• 1240520-29-9 3,5-di-(decyloxy)benzoic acid N-3,4,5-tri-(decyloxy)benzoyl hydrazide 

Relevant articles and documents

3,5-Dialkoxy Substituted Triphenyl-tristriazolotriazines: Fluorescent Discotic Liquid Crystals

Tristriazolotriazines with a threefold 3,5-dialkoxyphenyl substitution were prepared from the corresponding phenyltetrazoles and cyanuric chloride. These star-shaped compounds are discotic liquid crystals that form broad and stable thermotropic mesophases

Hybrid photoluminescent materials containing a benzobisthiazole core for liquid crystal and gel applications

Tetra- and hexacatenar amide compounds containing a linear centrosymmetric benzobisthiazole core were synthesized with good yields. These compounds were characterized and their structures confirmed by elemental analysis, and FT-IR, Maldi mass and NMR spectroscopy. All compounds exhibited excellent thermal stability up to 330 °C. The tetracatenar series containing a double substitution in the meta positions did not show mesomorphic behaviour, whereas the hexacatenar and tetracatenar series having a double substitution in the meta and para positions showed liquid crystal properties with optical textures typical of columnar mesophases corroborated by POM analysis. The mesomorphic properties were dependent on the length, number and position of alkoxy chains attached at the end of the rigid core. XRD studies of the hexacatenar series showed the hexagonal columnar structure of the mesophases. Photoluminescence properties in solution were observed in the visible region, with good quantum yields. In the solid state, these compounds behave as blue emitters and they are able to change colour with acid or base addition. The hexacatenar benzobisthiazole compound with an alkoxy chain of 14 carbons presented properties of a supergelator in chloroform, leading to the formation of a fluorescent organogel material with fluorescence emission in the blue region.

Microwave-assisted synthesis, structure, and tunable liquid-crystal properties of 2, 5-diaryl-1, 3, 4-thiadiazole derivatives through peripheral n-alkoxy chains

A series of substituted 2, 5-diaryl-1, 3, 4-thiadiazole derivatives are prepared by microwave-assisted synthesis in the absence of an organic solvent. All derivatives are well characterized by 1H and 13C NMR, MS, and elemental analys