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16β-Morpholino-3β-hydroxy-5α-androstan-17-one is a synthetic steroidal compound that belongs to the class of androgens, which are male sex hormones. This specific compound is characterized by the presence of a morpholine ring at the 16β position, a hydroxyl group at the 3β position, and a ketone group at the 17-one position. It is structurally similar to testosterone, the primary male sex hormone, but with modifications that can alter its biological activity. 16β-morpholino-3β-hydroxy-5α-androstan-17-one is of interest in the field of medicinal chemistry and endocrinology, as it may have potential applications in the development of drugs for treating conditions related to androgen deficiency or imbalance. The specific effects and uses of 16β-morpholino-3β-hydroxy-5α-androstan-17-one are subject to ongoing research, and its properties may be compared to those of other androgens to understand its potential therapeutic value.

3000-34-8

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3000-34-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3000-34-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,0 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3000-34:
(6*3)+(5*0)+(4*0)+(3*0)+(2*3)+(1*4)=28
28 % 10 = 8
So 3000-34-8 is a valid CAS Registry Number.

3000-34-8Downstream Products

3000-34-8Relevant academic research and scientific papers

Stereospecific Synthesis of 16α-Hydroxy-17-oxo Steroids by Controlled Alkaline Hydrolysis of Corresponding 16-Bromo 17-Ketones and Its Reaction Mechanism

Numazawa, Mitsuteru,Nagaoka, Masao

, p. 4024 - 4029 (1982)

Synthesis of 16α-hydroxy-17-oxo steroids 3, 5b, and 3β,16α-dihydroxy-5-17-oxoandrosten-3-yl sulfate (7) from 16α-bromo-17-oxo steroids 1, 5a, and 6a and the reaction mechanism of the controlled alkaline hydrolysis are described.Treatment of the bromo ketones with NaOH in aqueous DMF gave the 16α-hydroxy 17-ketones stereoselectively in 95percent yield without formation of other ketols.The sodium salt of 3-sulfate 7 was also obtained in one step in 85percent yield from the corresponding bromo ketone (1a).Isotope-labeling experiments and time-course studies showed that equilibration between the 16-bromo epimers 1 and 2 precedes the formation of 3, in which the true intermediate is 2 and not 1, and that the ketol 3 is formed by the direct SN2 displacement of the 16β-bromine.The 16β-morpholino derivative 8 obtained by reaction of 1 with morpholine was shown to be an isomerized product of the 16α isomer which is produced also by SN2 displacement of the 16β-bromine.The mechanism of ketol rearrangement of 3 to the 17β-hydroxy-16-oxo compound 4 was found to involve a hydration to the carbonyl function.The new hydration-dehydration mechanism is proposed for the ketol rearrangement.

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