131525-50-3

Basic information

• Product Name: 3',4'-(DIOCTYLOXY)BENZALDEHYDE
• Synonyms: 3',4'-(DIOCTYLOXY)BENZALDEHYDE;3',4'-(Dioctyloxy)benzaldehyde, 99+%;3,4-Bis(octyloxy)benzaldehyde;3,4-(Dioctyloxy)benzaldehyde, min.
• CAS NO: 131525-50-3
• Molecular Formula: C₂₃H₃₈O₃
• Molecular Weight: 362.55
• Mol File: 131525-50-3.mol
• Article Data: 30

Chemical Properties

• Melting Point: 54-56 °C
• Boiling Point: 454.13°C (rough estimate)
• Flash Point: 232.1 °C
• Appearance: beige flakes
• Density: 0.9775 (rough estimate)
• Refractive Index: 1.5480 (estimate)
• CAS DataBase Reference: 3',4'-(DIOCTYLOXY)BENZALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 3',4'-(DIOCTYLOXY)BENZALDEHYDE(131525-50-3)
• EPA Substance Registry System: 3',4'-(DIOCTYLOXY)BENZALDEHYDE(131525-50-3)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 37/39-26
• Hazardous Substances Data: 131525-50-3(Hazardous Substances Data)

Upstream product

• 629-27-6 1-Iodooctane 
• 139-85-5 3,4-dihydroxybenzaldehyde 
• 111-83-1 1-bromo-octane 

Downstream Products

• 1360882-46-7 C₃₉H₅₁N₃O₂ 
• 1360882-51-4 2,6-bis-(4(4,6-O-ethylidene-β-D-glucopyranosyl-amino)phenyl)-4-(3,4-di-O-octyl-phenyl)pyridine 
• 1360882-52-5 2,6-bis-(4(4,6-O-butylidene-β-D-glucopyranosyl-amino)phenyl)-4-(3,4-di-O-octyl-phenyl)pyridine 
• 1415488-06-0 C₃₀H₄₃NO₄ 
• 131525-56-9 3,4-bis(octyloxy)benzoic acid 
• 1048966-21-7 1,2-bis(octyloxy)-4-ethynyl-benzene 

Relevant articles and documents

Investigation of iron(III) ionic structural complexes for seebeck coefficient enhancement using variation of ligand lengths with extended Π-conjugated bipyridyl ligands

Five new octahedral spin-crossover magnetic complexes with general formulae, [Fe(LCn)3](BF4)3, where L = ligand, and n = 8, 10, 12, 14, 16, were synthesized and characterized. The influence of different ligand lengths on t

Molecular design strategies for spin-crossover (SCO) metal complexes (Fe(II) and Co(II)) for thermoelectricity

TEC are developing technology to generate electricity from thermal energy. It causes current flow when redox solution disturbs the electrochemical potential equilibrium between the electrolyte and two inert electrodes upon application of a temperature gra

Synthesis and mesomorphic characterization of some novel steroidal mesogens: A structure–property correlation

The steroidal derivatives are found to be extremely good mesogens since their inception. Because of their inherent chirality, they have the potential to induce a wide variety of liquid crystalline phases, including frustrated phases depending upon the structure of the steroidal skeleton and the substituents attached. In this report, a series of novel monoalkoxy and dialkoxy benzoate derivatives of ergosterol and a few monoalkoxy derivatives of stigmasterol have been synthesized and their mesomorphic property has been investigated. The derivatives exhibited various mesophases including SmA, SmC*, N*, TGB and blue phases. Also, the gelation ability of some of these derivatives with various organic solvents has been examined. Furthermore, the mesomorphism of these derivatives has been compared with the analogous cholesteryl counterparts.