70682-72-3 Usage
General Description
Tetradecyl benzoate is a chemical compound composed of a long hydrocarbon chain and a benzoic acid group. It is commonly used as an ingredient in many personal care products, such as skincare products and hair care products, as well as in industrial applications. Tetradecyl benzoate acts as an emollient, helping to soften and smooth the skin and hair, and also has antimicrobial properties, making it useful in formulations designed to prevent or treat bacterial or fungal infections. Additionally, it can act as a solvent and stabilizer in various formulations, helping to improve the overall performance and stability of products. Overall, tetradecyl benzoate is a versatile and multifunctional chemical that is widely used in the cosmetic and personal care industry.
Check Digit Verification of cas no
The CAS Registry Mumber 70682-72-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,6,8 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 70682-72:
(7*7)+(6*0)+(5*6)+(4*8)+(3*2)+(2*7)+(1*2)=133
133 % 10 = 3
So 70682-72-3 is a valid CAS Registry Number.
InChI:InChI=1/C21H34O2/c1-2-3-4-5-6-7-8-9-10-11-12-16-19-23-21(22)20-17-14-13-15-18-20/h13-15,17-18H,2-12,16,19H2,1H3
70682-72-3Relevant articles and documents
LiHMDS: Facile, highly efficient and metal-free transesterification under solvent-free condition
Gore, Kiran R.,Mittapelli, Lavanya L.
, (2020/10/27)
Transesterification is one of the important organic reactions employed in numerous industrial as well as laboratory applications for the synthesis of various esters. Herein, we report a rapid, highly efficient, and transition metal-free transesterification reaction in the presence of LiHMDS under solvent-free conditions. The transesterification reaction was carried out with three different benzoate esters and a wide range of primary and secondary alcohols (from C3-C18) in good to excellent yields (45 examples). By considering the commercial role of esters, this method will be promising for the facile synthesis of esters in industry-relevant applications.
