154845-72-4

Basic information

• Product Name: Benzoic acid, 4-(hexyloxy)-, ethyl ester
• CAS NO: 154845-72-4
• Molecular Formula: C15H22O3
• Molecular Weight: 250.338
• Mol File: 154845-72-4.mol
• Article Data: 17

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 4-(hexyloxy)-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 4-(hexyloxy)-, ethyl ester(154845-72-4)
• EPA Substance Registry System: Benzoic acid, 4-(hexyloxy)-, ethyl ester(154845-72-4)

Safety Data

• Hazardous Substances Data: 154845-72-4(Hazardous Substances Data)

Upstream product

• 120-47-8 Ethyl 4-hydroxybenzoate 
• 111-25-1 1-bromo-hexane 
• 99-96-7 4-hydroxy-benzoic acid 
• 111-27-3 hexan-1-ol 

Downstream Products

• 31792-05-9 p-Hexyloxybenzohydroxamsaeure 
• 77477-53-3 5,5'-Bis-<4-hexyloxy-phenyl>-2,2'-di-1,3,4-thiadiazol 
• 1184937-94-7 C₂₉H₃₈O₅ 
• 177424-32-7 4-(2`hydroxy-4`-hexylhydroxybenzoylhydroxy)benzaldehyde 
• 1630012-58-6 C₁₈H₂₉N₃O₃ 
• 1630012-44-0 C₁₄H₁₈N₂O₃ 
• 1630013-00-1 4-butyl-5-(4-hexyloxyphenyl)-2H-1,2,4-triazole-3(4H)-one 
• 1440507-30-1 tris[2-(4-hexyloxybenzoyloxy)ethyl]amine 

Relevant articles and documents

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.

Design and characterization of novel bis-benzamide liquid crystalline materials

A new homologous series of symmetric, bent-shaped bis-benzamide dimers have been prepared. Several 1,n-bis(p-aminophenoxy)alkanes (n = 3, 5, 9,10,11) were employed as spacers and p-hexyloxy tails have been synthesized and appended to the spacers by amide linking groups. Different important parameters were explored using computational analysis by semi empirical method. The experimental results were correlated with theoretical studies and relationship between molecular structure and mesogenic behavior has been established. The mesomorphic properties of the resultant dimers were characterized by differential scanning calorimetry (DSC) and polarized optical microscopy (POM) equipped with a hot stage. Change in mesomorphic properties with change of methylene spacers was observed. Enantiotropic mesogenic behavior was exhibited by D3A6, D10A6 and D11A6 and the needle like and blurred schleiren textures were observed. It was observed that increased methylene spacers chain length decreased the melting temperatures. Thermogravimetric analysis revealed the thermal stability of dimers upto 360 °C.

Tuning the self-assembly and photophysical properties of bi-1,3,4-thiadiazole derivatives through electron donor-acceptor interactions and their application in OLEDs

We report several shape anisotropic molecules that contain two centrally placed 1,3,4-thiadiazole units, which vary from each other with respect to the number and length of the flexible chains at the termini. The number, position and length of the periphe