5802-82-4

Usage

Uses

Used in Chemical Synthesis:
METHYL HEXACOSANOATE is used as an intermediate in special synthesis for its unique chemical properties, which make it a valuable component in the creation of various compounds.
Used in Medical Research:
METHYL HEXACOSANOATE is used as a reference standard in medical research, particularly in the field of gas chromatography. Its unique chemical properties allow for accurate analysis and identification of other compounds in various samples.
Used in Pharmaceutical Industry:
METHYL HEXACOSANOATE is used as a component in the development of new pharmaceuticals, thanks to its unique chemical properties and solubility in alcohol and ether.
Used in Analytical Chemistry:
METHYL HEXACOSANOATE is used as a reference standard in analytical chemistry, particularly in gas chromatography, to ensure accurate and reliable results in the identification and quantification of other compounds.

InChI:InChI=1/C27H54O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25-26-27(28)29-2/h3-26H2,1-2H3

Upstream product

• 186581-53-3 diazomethane 
• 506-46-7 1-hexacosanoic acid 
• 629-72-1 pentadecyl bromide 
• 929-33-9 methyl 11-iodoundecanoate 
• 67-56-1 methanol 
• 1490-25-1 succinic acid monomethylester chloride 
• 111514-83-1 4-(5-Octadecyl-thiophen-2-yl)-4-oxo-butyric acid methyl ester 
• 102945-07-3 2-octadecylthiophene 
• 111514-94-4 3-[2-(5-Octadecyl-thiophen-2-yl)-[1,3]dithiolan-2-yl]-propionic acid methyl ester 

Downstream Products

• 506-52-5 hexacosyl alcohol 
• 506-46-7 1-hexacosanoic acid 

Relevant academic research and scientific papers

Dammarane triterpenoids from Carnauba, Copernicia prunifera (Miller) H. E. Moore (Arecaceae), wax

Phytochemical investigation from carnauba (Copernicia prunifera) wax led to the identification of sixteen dammarane–type triterpenes, including thirteen new characterized as: (24R*)-methyldammara-20,25-dien-3α-ol and a mixture of alkyl (24R*)-methyldammar-25-en-20-ol-3β-carboxylates, together with three previously described triterpenes: carnaubadiol, (24R*)-methyldammara-20,25-dien-3β-ol and (24R*)-24-methyldammara-20,25-dien-3-one. Moreover, four fatty alcohols (eicosanol, docosanol, tetracosanol and hexacosanol) as well as four sterols (cholesterol, campesterol, stigmasterol, and sitosterol) were also obtained. These compounds were isolated using classical chromatographic methods and their structures were determined by spectroscopic and chemical methods.

A New Synthesis of Long Chain Acid Esters and Carbinols

A versatile synthesis of difficulty accessible long chain acid esters and carbinols is described.The synthesis involves acylations at 2- and 5-positions of thiophene.Thioketalation of the resulting ketoesters followed by Raney nickel desulfurization yield acid esters which on LAH reduction give the corresponding carbinols.

ALIPHATIC CONSTITUENTS FROM DUBOISIA MYOPOROIDES

Four new compounds, isolated from the leaves and stem of Duboisia myoproides have been characterized as 6-methyldotriacontane, hentriacontanyl tetratriacontanoate, 3-hydroxydotriacontan-28-one and 4-pentatriacontanone, respectively, by spectral data and chemical studies.Key Word Index - Duboisia myoporoides; Solanaceae; leaves and stems; 6-methyldotriacontane; hentriacontanyl tetratriacontanoate; 3-hydroxydotriacontan-28-one; 4-pentatriacontanone.