853055-43-3

Basic information

• Product Name: Benzoyl chloride, 3,4,5-tris(tetradecyloxy)-
• CAS NO: 853055-43-3
• Molecular Formula: C49H89ClO4
• Molecular Weight: 777.696
• Mol File: 853055-43-3.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: Benzoyl chloride, 3,4,5-tris(tetradecyloxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoyl chloride, 3,4,5-tris(tetradecyloxy)-(853055-43-3)
• EPA Substance Registry System: Benzoyl chloride, 3,4,5-tris(tetradecyloxy)-(853055-43-3)

Safety Data

• Hazardous Substances Data: 853055-43-3(Hazardous Substances Data)

Upstream product

• 121-79-9 Propyl gallate 
• 402912-75-8 3,4,5-tristetradecyloxybenzoic acid propyl ester 
• 112-71-0 1-Bromotetradecane 
• 99-24-1 methyl galloate 
• 831-61-8 Ethyl gallate 
• 149-91-7 3,4,5-trihydroxybenzoic acid 
• 1020178-14-6 3,4,5-tris(tetradecyloxy)benzoic acid ethyl ester 
• 219993-13-2 methyl [3,4,5-tris(n-tetradecan-1-yloxy)]benzoate 
• 179031-22-2 3,4,5-tris(tetradecyloxy)benzoic acid 

Downstream Products

• 350015-50-8 4'-hydroxybiphenyl-4-[3,4,5-tris(tetradecyloxy)benzoate] 
• 1268837-84-8 C₅₅H₉₃NO₇ 
• 1264293-50-6 C₅₅H₉₅NO₅ 
• 1201762-55-1 6-bromohexyl 3,4,5-tris(tetradecyloxy)benzoate 
• 1201762-73-3 [1,1'-biisoquinolin]-4,4'-diyl bis[3,4,5-tris(tetradecyloxy)benzoate] 
• 1151760-17-6 2,6-bis(3,4,5-tritetradecyloxyphenyl)benzo[1,2-d;5,4-d']bisoxazole 
• 942150-61-0 3'-chloro-4'-hydroxybiphenyl 4-[2-chloro-3,4,5-tri(tetradecyloxy)]benzoate 
• 942150-60-9 4'-hydroxybiphenyl 4-[2,6-dichloro-3,4,5-tri(tetradecyloxy)]benzoate 
• 942150-59-6 4'-hydroxybiphenyl 4-[2-chloro-3,4,5-tri(tetradecyloxy)]benzoate 
• 502623-27-0 [4,4-bis-(4-amino-3,5-dimethyl-phenyl)-piperidin-1-yl]-(3,4,5-tris-tetradecyloxy-phenyl)-methanone 

Relevant articles and documents

Control the self-assembly of fluorenone-based polycatenars by tuning chain length

Using Suzuki coupling reactions as key steps, a series of fluorenone-based polycatenars, consisting of a central 2,7-diphenyl-9-fluorenone core connected with the 3,4,5-trialkoxybenzoate unit via –COO- linkage at each side have been synthesized. Upon elon

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.

Columnar liquid-crystalline phase from a series of symmetrical bent diphenylamine derivatives: Synthesis and characterization

A series of symmetrical bent-shaped materials with six alkoxy chains at the terminal position has been designed and synthesized. All except one exhibit columnar mesophase behavior. The mesomorphic properties of the compounds have been studied with the help of polaralizing optical microscopy (POM) and differential scanning colorimetry (DSC) experiments.