111195-34-7

Basic information

• Product Name: 3,4-Bis-octyloxy-benzoic acid ethyl ester
• Synonyms: 3,4-Bis-octyloxy-benzoic acid ethyl ester
• CAS NO: 111195-34-7
• Molecular Weight: 406.606
• Mol File: 111195-34-7.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 3,4-Bis-octyloxy-benzoic acid ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4-Bis-octyloxy-benzoic acid ethyl ester(111195-34-7)
• EPA Substance Registry System: 3,4-Bis-octyloxy-benzoic acid ethyl ester(111195-34-7)

Safety Data

• Hazardous Substances Data: 111195-34-7(Hazardous Substances Data)

Upstream product

• 111195-33-6 3,4-di-n-octyloxyacetophenone 
• 120-80-9 benzene-1,2-diol 
• 4956-41-6 1,2-dioctyloxybenzene 
• 111-83-1 1-bromo-octane 
• 3943-89-3 Ethyl protocatechuate 
• 64-17-5 ethanol 
• 131525-56-9 3,4-bis(octyloxy)benzoic acid 

Downstream Products

• 131525-80-9 3,4-Bis-octyloxy-benzoic acid 4-hydroxy-phenyl ester 
• 131525-71-8 3,4-Bis-octyloxy-benzoic acid 4-benzyloxy-phenyl ester 
• 134766-01-1 3,4-Bis-octyloxy-benzoyl chloride 
• 1184937-18-5 C₄₉H₇₈O₇ 
• 1435464-94-0 C₇₄H₉₄N₄NiO₁₀ 

Relevant articles and documents

Fluorescence-enhanced organogels and mesomorphic superstructure based on hydrazine derivatives

New low-molecular-mass organic gelators (LMOGs) bearing hydrazine linkage and end-capped by phenyl, namely 1,4-bis[(3,4-bisalkoxyphenyl)hydrozide] phenylene (BPH-n, n = 4, 6, 8, 10), were designed and synthesized. These organogelators have shown great ability to gel a variety of organic solvents to form stable organogels with the critical gelation concentration as low as 8.7 × 10-4 mol L-1 (0.06 wt %). The formed gel has a high gel-sol transition temperature (Tgel) at low gelation concentration. Aggregation-induced emission (AIE) has been observed after gelation though conventional chromophore units not incorporated inBPH-n. The fluorescence quantumyields of xerogel are 2 orders higher than that of dilute solution. In addition, the BPH-n (n=6, 8, 10) exhibited thermotropic hexagonal column (Colh) mesophase, which are stable at room temperature as revealed by differential scanning calorimetry (DSC), polarized optical microscopy (POM), and X-ray diffraction (XRD) studies.

Synthesis and characterization of bis [ n -(4-benzoyloxy) Benzylidene{ n (n -di-/tri-alkoxy)benzoyl}-hydrazinato]nickel(II) complexes displaying liquid crystalline columnar phases

A series of materials based on the aroylhydrazinatonickel (II) complex is synthesized and characterized. The molecule in the materials consist of two 4-benzoyloxy-benzene groups and two benzene rings having two or three alkoxy chains containing 6, 8, 10,

The synthesis and mesomorphism of di-, tetra- and hexa-catenar liquid crystals based on 2,2′-bipyridine

2,2′-Bipyridines are known to coordinate to a wide variety of metal centres. In this paper, liquid-crystalline two-chained (dicatenar), four-chained (tetracatenar) and six-chained (hexacatenar) bipyridines are synthesised and their mesomorphism is described. For the tetracatenar bipyridines, a full homologous series, from tetramethoxy to tetratetradecyloxy, was synthesised, and the phase diagram showed a classic progression from nematic and smectic C phases at short chain length, through a cubic phase to a columnar phase.