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Δ4-Pregnen-11β,21-diol-3,20-dione di-p-fluorobenzoate is a complex organic compound with the molecular formula C31H34F2O6. It is a derivative of pregnane, a class of steroid compounds, and features a pregnane core with two hydroxyl groups at the 11β and 21 positions, and ketone groups at the 3 and 20 positions. The compound is further characterized by the presence of two p-fluorobenzoate groups, which are attached to the molecule, likely through esterification. This chemical structure suggests that it may have potential applications in pharmaceuticals or as an intermediate in the synthesis of other steroidal compounds. The specific biological activity or therapeutic use of Δ4-pregnen-11β,21-diol-3,20-dione di-p-fluorobenzoate would depend on its ability to interact with various biological targets, such as hormone receptors, which could be explored through further research and development.

92010-59-8

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92010-59-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92010-59-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,0,1 and 0 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 92010-59:
(7*9)+(6*2)+(5*0)+(4*1)+(3*0)+(2*5)+(1*9)=98
98 % 10 = 8
So 92010-59-8 is a valid CAS Registry Number.

92010-59-8Downstream Products

92010-59-8Relevant academic research and scientific papers

Characterization of amino acids and steroids by fluorine-19 nuclear magnetic resonance spectrometry of p-fluorobenzoyl derivatives

Spratt,Meng,Dorn

, p. 76 - 81 (2007/10/02)

The utility of p-fluorobenzoyl chloride as an analytical **1**9F NMR reagent to characterize sterols and amino acids is reported. The **1**9F chemical shift data for approximately 30 sterols and amino acids are presented. The interaction of the p-fluorobenzoyl group with the steroid ring system makes a significant contribution to the **1**9F chemical shift of these steroid derivatives. These results suggest a convenient technique for characterizing different steroids (e. g. , estrogens, pregnanes, androstanes, etc. ).

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