177715-63-8

Basic information

• Product Name: Benzoic acid, 4-(pentyloxy)-, ethyl ester
• CAS NO: 177715-63-8
• Molecular Formula: C14H20O3
• Molecular Weight: 236.311
• Mol File: 177715-63-8.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 4-(pentyloxy)-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 4-(pentyloxy)-, ethyl ester(177715-63-8)
• EPA Substance Registry System: Benzoic acid, 4-(pentyloxy)-, ethyl ester(177715-63-8)

Safety Data

• Hazardous Substances Data: 177715-63-8(Hazardous Substances Data)

Upstream product

• 99-96-7 4-hydroxy-benzoic acid 
• 71-41-0 pentan-1-ol 
• 120-47-8 Ethyl 4-hydroxybenzoate 
• 110-53-2 1-Bromopentane 

Downstream Products

• 107265-33-8 1,3-Di-(p-n-pentyloxyphenyl)propane-1,3-dione 
• 1630012-57-5 C₁₇H₂₇N₃O₃ 
• 1630012-43-9 C₁₃H₁₆N₂O₃ 
• 1630012-97-3 4-butyl-5-(4-pentyloxyphenyl)-2H-1,2,4-triazole-3(4H)-one 
• 64328-62-7 4-pentyloxybenzoyl hydrazide 
• 36823-84-4 4-pentyloxybenzoyl chloride 
• 33903-95-6 C₃₃H₄₀O₆ 
• 33905-70-3 C₂₆H₂₆O₆ 
• 33905-63-4 4-hydroxyphenyl 4-amyloxybenzoate 
• 15872-41-0 4-(pentyloxy)benzoic acid 

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.

Oxime Carbamate-Discovery of a series of novel FAAH inhibitors

A series of novel oxime carbamates have been identified as potent inhibitors of the key regulatory enzyme of the endocannabinoid signaling system, fatty acid amide hydrolase (FAAH). In this Letter, the rationale behind the discovery and the biological evaluations of this novel class of FAAH inhibitors are presented. Both in vitro and in vivo results of selected targets are discussed, along with inhibition kinetics and molecular modeling studies.1.

Synthesis and gelation behavior of 4′-propyl-1,1′- bi(cyclohexyl)-4-one 4-alkoxybenzoylhydrazone

A series of new alkoxybenzoylhydrazones of 4′-propyl-1,1′- bi(cyclohexyl)-4-one were prepared as novel low molecular weight organogelators (LMOGs). Their gelation behaviors in 10 solvents were tested. Some of the compounds could form stable gels in bulk o