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Stigmast-5-en-3β-yl-(tetra-O-acetyl-β-D-glucopyranoside) is a complex organic compound that belongs to the class of steroids. It is characterized by a steroidal nucleus with a hydroxyl group at the 3β position, which is glycosidically linked to a tetra-O-acetyl-β-D-glucopyranoside moiety. This means that the glucose molecule is attached to the steroid through its β-anomeric configuration, and all four hydroxyl groups of the glucose are acetylated, which protects them from unwanted reactions. stigmast-5-en-3β-yl-(tetra-O-acetyl-β-D-glucopyranoside) is of interest in the field of organic chemistry and may have potential applications in pharmaceuticals or as a chemical intermediate due to its unique structure and reactivity.

4282-00-2

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4282-00-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4282-00-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,8 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4282-00:
(6*4)+(5*2)+(4*8)+(3*2)+(2*0)+(1*0)=72
72 % 10 = 2
So 4282-00-2 is a valid CAS Registry Number.

4282-00-2Downstream Products

4282-00-2Relevant 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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