41371-14-6 Usage
General Description
Cholesterol N-butyl carbonate is a chemical compound that is derived from cholesterol, a waxy substance found in the cells of the body. It is a synthetic form of cholesterol that is modified by adding a butyl group to the carbon atom. This modification alters the properties of cholesterol, making it more soluble in organic solvents. Cholesterol N-butyl carbonate is commonly used in the pharmaceutical industry as an ingredient in drug formulations, particularly in the development of lipid-based drug delivery systems. Its ability to enhance the solubility and bioavailability of certain drugs makes it a valuable component in the development of new therapeutic agents. Additionally, it may have potential applications in the development of novel biomaterials for drug delivery and tissue engineering.
Check Digit Verification of cas no
The CAS Registry Mumber 41371-14-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,3,7 and 1 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 41371-14:
(7*4)+(6*1)+(5*3)+(4*7)+(3*1)+(2*1)+(1*4)=86
86 % 10 = 6
So 41371-14-6 is a valid CAS Registry Number.
InChI:InChI=1/C32H54O3/c1-7-8-20-34-30(33)35-25-16-18-31(5)24(21-25)12-13-26-28-15-14-27(23(4)11-9-10-22(2)3)32(28,6)19-17-29(26)31/h12,22-23,25-29H,7-11,13-21H2,1-6H3/t23-,25+,26+,27-,28+,29+,31+,32-/m1/s1
41371-14-6Relevant articles and documents
Cycling of waste fusel alcohols from sugar cane industries using supercritical carbon dioxide
Pereira,Pereira,Crédito,Gir?o,Idehara,González
, p. 81515 - 81522 (2015)
The present study describes the clean synthesis of non-phosgene organic carbonates (NPOCs) from a selective multicomponent reaction with two important by-products from sugar and alcohol industries, namely, fusel alcohols and carbon dioxide, in the presence of 1,8-diazabicycloundecene (DBU), 1,5-diazabicyclo[4.3.0]-non-5-ene (DBN) or 1,3,4,6,7,8-hexahydro-2H-pyrimido[1,2-a]-pyrimidine (TBD) and an alkylating agent. The bases were used for the nucleophilic activation of the alcohols. The synthesis of carbonates was carried out without solvent and confirmed by GC-MS with EI ionization mode, 1H- and 13C-NMR and FT-IR analysis. The carbonates were obtained in excellent yields. Crude fusel alcohol can be converted to alkylcarbonates. The proposed methodology can also be employed to convert other hydroxylated compounds into carbonates.
