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β-Sitosteryl bromide, also known as β-sitosterol bromide, is a chemical compound derived from the plant sterol β-sitosterol. It is a white crystalline solid with the chemical formula C29H47BrO and a molecular weight of 471.68 g/mol. β-sitosteryl bromide is used in various applications, including pharmaceuticals, as an intermediate in the synthesis of other compounds, and in research studies. It is known for its potential anti-inflammatory and cholesterol-lowering properties, which are being investigated for their potential health benefits. β-Sitosteryl bromide is typically obtained through the bromination of β-sitosterol, a process that involves the reaction of β-sitosterol with bromine in an organic solvent.

66252-73-1

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66252-73-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66252-73-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,2,5 and 2 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 66252-73:
(7*6)+(6*6)+(5*2)+(4*5)+(3*2)+(2*7)+(1*3)=131
131 % 10 = 1
So 66252-73-1 is a valid CAS Registry Number.

66252-73-1Downstream Products

66252-73-1Relevant academic research and scientific papers

SYNTHESIS OF TRITERPENE AND STEROID GLYCOSIDES

Uvarova, Nina I.,Atopkina, Lyubov N.,Elyakov, Georgi B.

, p. 33 - 42 (2007/10/02)

The glycosylation of cholesterol, β-sitosterol, 28-O-acetylbetulin, and betulin with acylated glycosyl halides in the presence of Hg(OAc)2, Hg(CN)2, CdCO3, Ag2O, Ag2CO3, and HgO + HgBr2 usually gives acylated αβ-glycosides accompanied by acetates, ethers, and bromo and unsaturated derivatives of the initial alcohols.The use of Hg(CN)2 gave mainly β anomers (40-87percent), whereas α anomers preponderated when Hg(OAc)2 was the catalyst.When there was a deficiency of hydrogen halide acceptor and in the presence of the acidic catalyst HgBr2*HBr, the β anomer, produced initially, underwent anomerisation.Cholesteryl α-D-glucopyranoside tetra-acetate (48percent) was obtained by anomerisation of the β anomer.

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