154845-73-5

Basic information

• Product Name: Benzoic acid, 4-(heptyloxy)-, ethyl ester
• CAS NO: 154845-73-5
• Molecular Formula: C16H24O3
• Molecular Weight: 264.365
• Mol File: 154845-73-5.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 4-(heptyloxy)-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 4-(heptyloxy)-, ethyl ester(154845-73-5)
• EPA Substance Registry System: Benzoic acid, 4-(heptyloxy)-, ethyl ester(154845-73-5)

Safety Data

• Hazardous Substances Data: 154845-73-5(Hazardous Substances Data)

Usage

General Description

Benzoic acid, 4-(heptyloxy)-, ethyl ester, also known as ethyl 4-heptyloxybenzoate, is an ester compound with the molecular formula C14H20O3. It is a clear, colorless liquid that is insoluble in water but soluble in organic solvents. This chemical is commonly used as a flavoring agent in food and beverages, as well as a fragrance ingredient in perfumes and personal care products. It also has potential applications in the pharmaceutical and agrochemical industries. Ethyl 4-heptyloxybenzoate is known for its pleasant aroma and is used to impart a fruity, sweet, and floral note to various products. However, it is important to use this chemical in appropriate concentrations, as it may cause skin and eye irritation in high amounts.

Upstream product

• 111-70-6 n-heptan1ol 
• 99-96-7 4-hydroxy-benzoic acid 
• 120-47-8 Ethyl 4-hydroxybenzoate 
• 629-04-9 1-Bromoheptane 

Downstream Products

• 15872-42-1 4-heptyloxybenzoic acid 
• 1454572-01-0 C₃₀H₃₂N₂O₄S 
• 1630012-59-7 C₁₉H₃₁N₃O₃ 
• 1630012-45-1 C₁₅H₂₀N₂O₃ 
• 1630013-03-4 4-butyl-5-(4-heptyloxyphenyl)-2H-1,2,4-triazole-3(4H)-one 
• 56800-32-9 4-(4'-heptyloxybenzoyloxy)benzaldehyde 
• 40782-54-5 4-heptyloxybenzoyl chloride 
• 33903-99-0 C₃₅H₄₄O₆ 
• 33903-96-7 C₃₃H₄₀O₆ 
• 33905-72-5 C₂₈H₃₀O₆ 
• 33905-65-6 4-hydroxyphenyl 4-(heptyloxy)benzoate 
• 64328-64-9 4-heptyloxybenzoic hydrazide 
• 107265-34-9 1,3-Di-(p-n-heptyloxyphenyl)propane-1,3-dione 

Relevant articles and documents

Synthesis and anticonvulsant activity evaluation of 4-butyl-5-(4- alkoxyphenyl)-2H-1,2,4-triazole-3(4H)-ones

A series of 4-butyl-5-(4-alkoxyphenyl)-2H-1,2,4-triazole-3(4H)-ones (6a-6u) was designed and synthesized. The anticonvulsant effects and neurotoxicity of the compounds were evaluated with maximal electroshock test and rotarod test. Among the synthetic compounds, 4-butyl-5-(4-(2-fluorinebenzyl)phenyl)-2H-1,2,4- triazole-3 (4H)-one (6k) was the most potent with ED50 value of 27.4 mg/kg and protective index (PI = TD50/ED50) value of 12.0. Besides the anti-MES efficacy, the potency of compound 6k against seizures induced by pentylenetetrazole (PTZ), 3-mercaptopropionic acid (3-MP), and bicuculline (BIC) was also established, which suggested that the mechanisms of action including enhancing of GABAergic activity might be involved in its anticonvulsant activity.

A new way to access chiral liquid crystals: Organocatalyst-mediated synthesis of chiral rod-like liquid crystals

In this article, an asymmetric organocatalytic way to prepare chiral liquid crystals from non-chiral starting materials was described. By using L-proline as the organocatalyst, several new chiral rod-like liquid crystals that are elusive with traditional methods were prepared. In addition, a series of novel enone-containing rod-like liquid crystals were also obtained as side-products. Mesomorphic properties of all new compounds were studied by Polarized Optical Microscope and Differential Scanning Calorimetry. Copyright Taylor & Francis Group, LLC.

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.