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β-Sitosteryl 2,3,4,6-tetra-O-acetyl-α-D-glucopyranoside is a complex organic compound that belongs to the class of sterols. It is a derivative of β-sitosterol, a plant sterol that is structurally similar to cholesterol. This specific compound is characterized by the presence of a β-sitosterol molecule that has been esterified with four acetyl groups at the 2, 3, 4, and 6 positions of the α-D-glucopyranoside sugar moiety. The acetyl groups are short-chain fatty acid derivatives that contribute to the compound's lipophilic nature, which can affect its solubility and biological activity. β-sitosteryl 2,3,4,6-tetra-O-acetyl-α-D-glucopyranoside is of interest in the field of chemistry and biochemistry, particularly in studies related to the synthesis and properties of sterol derivatives, as well as their potential applications in pharmaceuticals and nutraceuticals.

66252-74-2

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66252-74-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66252-74-2 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 4 respectively.
Calculate Digit Verification of CAS Registry Number 66252-74:
(7*6)+(6*6)+(5*2)+(4*5)+(3*2)+(2*7)+(1*4)=132
132 % 10 = 2
So 66252-74-2 is a valid CAS Registry Number.

66252-74-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name β-sitosterolin tetraacetate

1.2 Other means of identification

Product number -
Other names β-sitosterol-tetraacetyl-β-D-glucopyranoside

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:66252-74-2 SDS

66252-74-2Downstream Products

66252-74-2Relevant 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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