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3β-acetoxy-5α-hydroxycholestan-6-one is a steroidal compound characterized by a cholestane skeleton, which is a derivative of cholesterol. This specific molecule features a hydroxyl group at the 5α position, an acetoxy group at the 3β position, and a ketone group at the 6 position. The acetoxy group indicates the presence of an acetylated hydroxyl group, which can influence the compound's reactivity and solubility. The 5α-hydroxyl group suggests that one of the hydroxyl groups is oriented in the α-configuration, which is important for understanding its stereochemistry. The ketone group at the 6 position adds to the compound's functional group diversity. This molecule is of interest in the field of organic chemistry, particularly in the study of steroidal compounds, which have various biological activities and are found in a wide range of natural products and pharmaceuticals.

6580-09-2

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6580-09-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6580-09-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,8 and 0 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6580-09:
(6*6)+(5*5)+(4*8)+(3*0)+(2*0)+(1*9)=102
102 % 10 = 2
So 6580-09-2 is a valid CAS Registry Number.

6580-09-2Upstream product

6580-09-2Relevant academic research and scientific papers

5β,6β-Epoxidation of 3β-Cholesteryl Acetate and its Analogues

Galagovsky, L. R.,Burton, G.,Gros, E. G.

, p. 806 - 810 (2007/10/02)

The treatment of acetylated Δ5-steroids with chromyl diacetate at low temperature afforded the 5β,6β-epoxy derivatives with stereoselectivity greater than 90 per cent. - keywords: Cholesterol, Sitosterol, Campesterol, Stigmasterol, Pregnenolone, Stereoselective Epoxidation

Action of N-Bromosuccinimide on Cholesteryl Acetate in Dimethyl Sulfoxide

Pradhan, Bhim Prasad,Ray, Tandra,Sharma, Bimal Prasad

, p. 846 - 848 (2007/10/02)

Cholesteryl acetate (1) on oxidation with NBS in DMSO furnishes six different compounds which have been identified as 5α-bromo-6-keto-cholestan-3β-yl acetate (2), 6α-bromo-5β-hydroxycoprostan-3β-yl acetate (3), 5α-hydroxy-6-keto-cholestan-3β-yl acetate (4), 5α,6β-dihydroxycholestan-3β-yl acetate (5), 3β,5α-dihydroxycholestan-6-one (6) and cholestane-3β,5α,6β-triol (7) by chemical studies and spectral (IR, mass, PMR, 13C NMR) data.Compound 3 is perhaps reported for the first time.

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