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β-(3-(benzyloxy)-17β-hydroxyestra-1,3,5(10)-triene)tricarbonylchromium is a complex organic compound that features a steroidal structure with a chromium tricarbonyl group attached. β-(3-(benzyloxy)-17β-hydroxyestra-1,3,5(10)-triene)tricarbonylchromium is derived from the estrane skeleton, which is a type of steroid, and is characterized by the presence of a benzyloxy group at the 3-position and a hydroxyl group at the 17β-position. The chromium tricarbonyl moiety, which consists of a chromium atom bonded to three carbon monoxide ligands, is known to stabilize certain organic compounds and can influence their chemical reactivity. This specific compound is of interest in the field of organometallic chemistry and may have potential applications in the development of new pharmaceuticals or materials science, given its unique structure and properties.

98757-32-5

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98757-32-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98757-32-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,7,5 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 98757-32:
(7*9)+(6*8)+(5*7)+(4*5)+(3*7)+(2*3)+(1*2)=195
195 % 10 = 5
So 98757-32-5 is a valid CAS Registry Number.

98757-32-5Relevant 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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