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α-(3-(benzyloxy)-17β-hydroxyestra-1,3,5(10)-triene)tricarbonylchromium is a complex organic compound that features a chromium atom bonded to three carbonyl groups and is part of the steroidal family, specifically an estrogen derivative. α-(3-(benzyloxy)-17β-hydroxyestra-1,3,5(10)-triene)tricarbonylchromium is characterized by a benzyloxy group attached to the 3-position of the estratriene backbone, which contributes to its chemical reactivity and potential applications in medicinal chemistry. The 17β-hydroxy group indicates the presence of a hydroxyl group at the 17β position, which is crucial for its biological activity. α-(3-(benzyloxy)-17β-hydroxyestra-1,3,5(10)-triene)tricarbonylchromium is of interest in the field of drug development, particularly for its potential role in modulating hormonal activity, and is studied for its structural and functional properties within the context of steroid chemistry.

98688-30-3

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98688-30-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98688-30-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,6,8 and 8 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 98688-30:
(7*9)+(6*8)+(5*6)+(4*8)+(3*8)+(2*3)+(1*0)=203
203 % 10 = 3
So 98688-30-3 is a valid CAS Registry Number.

98688-30-3Relevant academic research and scientific papers

Chromium tricarbonyl complexes of estradiol derivatives: Differentiation of α- and β-diastereoisomers using one- and two-dimensional NMR spectroscopy at 500 MHz

Top, Siden,Jaouen, Gérard,Vessières, Anne,Abjean, Jean-Pierre,Davoust, Daniel,Rodger, Charles A.,Sayer, Brian G.,McGlinchey, Michael J.

, p. 2143 - 2150 (2008/10/08)

The steroidal hormone β-estradiol and its derivatives in which the hydroxyl functionalities have been protected by benzyl or dimethyl-tert-butylsilyl groups bond to a tricarbonylchromium moiety via either the α- or the β-face of the arene ring. Unambiguous differentiation of these diastereomers is difficult without recourse to X-ray crystallographic techniques. These molecules have been characterized by 500-MHz 1H and 125-MHz 13C NMR spectroscopy; assignments are made by using the two-dimensional techniques COSY and SECSY as well as heteronuclear shift-correlated spectra. Thus, high field NMR spectroscopy provides a straightforward method of differentiating between the α- and β-isomers.

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