18000-76-5

Usage

Uses

Used in Pharmaceutical Industry:
3beta-(Methoxymethoxy)androst-5-en-17-one is used as a therapeutic agent for the treatment of hypogonadism and male infertility, addressing hormonal imbalances and promoting the development of male sexual characteristics.
Used in Sports and Bodybuilding:
Mestanolone is used as a performance-enhancing drug by athletes and bodybuilders for its anabolic properties, promoting muscle growth and increasing strength. However, its use is regulated and prohibited in competitive sports due to potential health risks and ethical concerns.
Used in Research:
3beta-(Methoxymethoxy)androst-5-en-17-one is utilized in scientific research to study the effects of androgens and anabolic steroids on various physiological processes, including muscle growth, bone density, and sexual development. This research helps in understanding the mechanisms of action and potential therapeutic applications of these compounds.

Upstream product

• 110535-48-3 (3S,8R,9S,10R,13S,14S,17S)-3-Methoxymethoxy-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl-cyanamide 
• 110535-45-0 (3S,8R,9S,10R,13S,14S,17S)-3-Methoxymethoxy-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-ylamine 
• 110535-54-1 (3S,8R,9S,10R,13S,14S)-3-Methoxymethoxy-10,13-dimethyl-1,2,3,4,7,8,9,10,11,12,13,14,15,16-tetradecahydro-cyclopenta[a]phenanthren-(17E)-ylidene-cyanamide 
• 53-43-0 dehydroepiandrosterone 
• 107-30-2 chloromethyl methyl ether 
• 109-87-5 Dimethoxymethane 
• 105644-82-4 Toluene-4-sulfonic acid (3S,10R,13S,17S)-3-methoxymethoxy-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl ester 
• 66168-96-5 3β-methoxymethoxy-5-androstene-17α-ol 

Downstream Products

• 173324-10-2 3β-methoxymethoxy-16α-phenylseleno-5-androsten-17-one 
• 105644-82-4 3β-Methoxymethoxy-5-androsten-17β-ol 17-p-Toluenesulfonate 
• 1624341-83-8 (3α,5α,6β,17β)-17-(benzyloxymethyl)-6-methoxy-3-(methoxymethoxy)-androstane 
• 1624341-82-7 (3α,5α,6β,17β)-17-(benzyloxymethyl)-6-methoxy-androstan-3-ol 
• 1624341-81-6 (5α,6β,17β)-17-(benzyloxymethyl)-6-methoxy-androstan-3-one 
• 1624341-80-5 (3β,5α,6β,17β)-17-(benzyloxymethyl)-6-methoxy-androstan-3-ol 
• 1624341-79-2 (3β,5α,6β,17β)-17-(benzyloxymethyl)-6-methoxy-3-(methoxymethoxy)-androstane 
• 1624341-78-1 (3β,5α,6β,17β)-17-(benzyloxymethyl)-3-(methoxymethoxy)-androstan-6-ol 
• 1624341-76-9 (3β,5α,17β)-17-(benzyloxymethyl)-3-(methoxymethoxy)-androstan-6-one 
• 1624341-75-8 (3β,17β)-17-(benzyloxymethyl)-3-methoxymethoxy-androst-5-ene 
• 53-43-0 dehydroepiandrosterone 

Relevant academic research and scientific papers

Dehydrogenation of Cyanamides. An Approach to Cyanimides and Carbonyl Compounds

Treatment of cyanamides with lead tetraacetate afforded the corresponding cyanimides in high yields.As these compounds can be readily and efficiently hydrolysed to carbonyl compounds; this sequence of reactions allows the synthesis of aldehydes and ketones from primary amines.

Synthesis of 3-Epi-6,7-dideoxyxestobergsterol A

3-Epi-6,7-dideoxyxestobergsterol A (2), an analogue of xestobergsterol A, has been synthesized from dehydroepiandrosterone (3) in 15 steps. The key synthetic intermediate, 15β,16α-dioxypregn-17(20)E-ene derivative 8, was prepared from the corresponding 15

Synthesis of 17-(isocyanotosylmethylene) steroids: precursors to pregnane derivatives

The synthesis is described of a series of twenty 17-(isocyanotosylmethylene) steroids 5 from 17-oxo steroids and 4-tolylsulfonylmethyl isocyanide (TosMIC).Furthermore, nine analogous 17-(isocyanosulfonylmethylene) steroids (15-21a) have been prepared usin

SYNTHESIS OF 2-PROPYNYL ETHERS OF STEROID ALCOHOLS

2-Propynyl ethers, derived from steroid alcohols with hydroxyl in position 3β, 17 or 20, were prepared by reaction with propargyl bromide and sodium hydroxide under conditions of phase transfer catalysis.Other hydroxy groups in the steroid molecule were protected with the methoxymethyl or 2-tetrahydropyranyl group.

INFRARED SPECTRA OF COMPOUNDS WITH THE METHOXYMETHYL PROTECTING GROUP

Infrared spectra of a series of compounds containing the CH3OCH2O- (MOM-O-) group have been studied.All the spectra exhibit three characteristic strong absorbtion bands due to coupled stretching vibrations of C-O-C-O-C grouping in the region 1200 - 1000 c