41755-79-7 Usage
General Description
Methyl dotriacontanoate, also known as methyl ester of docosanoic acid, is a chemical compound commonly found in natural substances such as plant oils and animal fats. It is a type of fatty acid ester, which is the result of the reaction between a fatty acid and an alcohol. Methyl dotriacontanoate is commonly used as a fragrance ingredient in cosmetic and personal care products, as well as in the production of soaps, detergents, and other household products. It has a waxy texture and is known for its moisturizing and emollient properties, making it a popular ingredient in skin and hair care products. Additionally, it is used as a lubricant in industrial applications and as a flavoring agent in food products.
Check Digit Verification of cas no
The CAS Registry Mumber 41755-79-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,7,5 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 41755-79:
(7*4)+(6*1)+(5*7)+(4*5)+(3*5)+(2*7)+(1*9)=127
127 % 10 = 7
So 41755-79-7 is a valid CAS Registry Number.
41755-79-7Relevant articles and documents
Bioactive phenylethanoids and coumarines from basalmocitrus cameroonensis
Wansi, Jean Duplex,Djouaka Bavoua, Judith Liliane,Happi, Emmanuel Ngeufa,Devkota, Krishna Prasad,Lenta, Bruno Ndjakou,Mesaik, Muhammed Ahmed,Choudhary, Muhammad Iqbal,Fomum, Zacharias Tanee,Sewald, Norbert
, p. 452 - 458 (2009)
Two new phenylethanoids, basalefhanoid A (1) and B (2), and one new ceramide, basalamide A (3), together with eleven known compounds (4-14) were isolated from the MeOH extract of the stem barks of Basalmocitrus cameroonensis. The structures of all compoun
A New Synthesis of Long Chain Acid Esters and Carbinols
Rao, S. Jagadishwar,Bhalerao, U. T.,Tilak, B. D.
, p. 208 - 211 (2007/10/02)
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.
