Interesting facts
Interesting Facts About 17-Acetoxy-17-ethynyl-13-methyl-... Acetate
This compound is a fascinating example of a complex synthetic organic molecule known for its structural intricacy and potential biological significance. As a chemical scientist, it's intriguing to explore its properties and applications:
- Steroid Derivative: This compound is a derivative of steroids, compounds that play crucial roles in biological systems, including hormones and vitamins.
- Chirality: The multiple chiral centers in the molecule make it an interesting subject for studies in stereochemistry, which is essential in pharmaceuticals as different stereoisomers can exhibit varying biological activities.
- Biological Activity: Due to its complex structure, this compound may exhibit significant hormonal and therapeutic activity, making it a potential candidate for drug development.
- Synthetic Pathways: The synthesis of this compound can involve intricate multistep reactions typical in organic chemistry, providing a rich ground for learning about reaction mechanisms and synthetic organic methodologies.
- Research and Applications: Exploring the potential applications of this compound could lead to innovations in medical research, particularly in understanding endocrine functions and developing treatments for hormone-related disorders.
In the world of chemistry, compounds like this challenge students and researchers alike to deepen their understanding of molecular interactions, synthesis, and biological significance. As Albert Einstein once said, "The most beautiful experience we can have is the mysterious." Engaging with such complex compounds can truly evoke a sense of wonder and discovery in the field of chemistry.
Synonyms
ETHYNODIOL DIACETATE
297-76-7
Femulen
Etynodiol Acetate
Continuin
Ethinodiol diacetate
Etynodiol diacetate
Etynodiol di(acetate)
Cervicundin
Ethynodiol diacetate [USAN]
Metrodiol
SC 11800
Luto-metrodiol
Metrodiol diacetate
SC-11800
19-Nor-17alpha-pregn-4-en-20-yne-3beta,17-diol diacetate
Ovulen 50
Ethynodiol (diacetate)
CHEBI:31580
DTXSID4020614
Ethynodiol acetate
(3beta,17beta)-17-ethynylestr-4-ene-3,17-diyl diacetate
[(3S,8R,9S,10R,13S,14S,17R)-17-acetyloxy-17-ethynyl-13-methyl-2,3,6,7,8,9,10,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate
NSC-759288
17alpha-Ethynyl-3,17-dihydroxy-4-estrene diacetate
17alpha-Ethynylestr-4-ene-3beta,17beta-diol acetate
3beta, 17beta-Diacetoxy-17alpha-ethynyl-4-oestrene
17alpha-Ethynyl-4-estrene-3beta,17beta-diol diacetate
DTXCID00614
3beta,17beta-Diacetoxy-19-nor-17alpha-pregn-4-en-20-yne
62H10A1236
19-Norpregn-4-en-20-yne-3,17-diol, diacetate, (3b,17a)-
ETHYNODIOL DIACETATE [MI]
ETHYNODIOL DIACETATE [JAN]
17alpha-Ethynyl-19-norandrost-4-ene-3beta,17-beta-diol diacetate
ETYNODIOL DIACETATE [MART.]
ETYNODIOL DIACETATE [WHO-DD]
ETHYNODIOL DIACETATE [USP-RS]
17alpha-ethynylestr-4-ene-3beta,17beta-diyl diacetate
19-norpregn-4-en-20-yn-3beta,17alpha-diol, diacetate
NCGC00166138-01
ETHYNODIOL DIACETATE [ORANGE BOOK]
ETHYNODIOL DIACETATE [USP IMPURITY]
ZOVIA COMPONENT ETHYNODIOL DIACETATE
ETHYNODIOL DIACETATE [USP MONOGRAPH]
KELNOR COMPONENT ETHYNODIOL DIACETATE
OVULEN COMPONENT ETHYNODIOL DIACETATE
(3S,8R,9S,10R,13S,14S,17R)-17-ethynyl-13-methyl-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene-3,17-diyl diacetate
19-Norpregn-4-en-20-yne-3,17-diol, diacetate, (3beta,17alpha)-
ETYNODIOL DIACETATE (MART.)
ETHYNODIOL DIACETATE (USP-RS)
CCRIS 305
ETHYNODIOL DIACETATE (USP IMPURITY)
ETHYNODIOL DIACETATE (USP MONOGRAPH)
8080 C. B.
19-Norpregn-4-en-20-yne-3,17-diol, diacetate, (3.beta.,17.alpha.)-
Ethynodiol diacetate [Progestins]
EINECS 206-044-9
17-alpha-Ethynyl-3,17-dihydroxy-4-estrene diacetate
3-beta, 17-beta-Diacetoxy-17-alpha-ethynyl-4-oestrene
17-alpha-Ethynylestr-4-ene-3-beta,17-beta-diol acetate
17-alpha-Ethynyl-4-estrene-3-beta,17-beta-diol diacetate
Ethynodiol diacetate (JAN/USP)
3-beta,17-beta-Diacetoxy-19-nor-17-alpha-pregn-4-en-20-yne
Ethynodiol diacetate [USAN:USP]
(3-beta,17-alpha)-19-Norpregn-4-en-20-yne-3,17-diol diacetate
17-alpha-Ethynyl-19-norandrost-4-ene-3-beta,17-beta-diol diacetate
UNII-62H10A1236
NCGC00186466-01
ethynodiol-diacetate
((3S,8R,9S,10R,13S,14S,17R)-17-acetyloxy-17-ethynyl-13-methyl-2,3,6,7,8,9,10,11,12,14,15,16-dodecahydro-1H-cyclopenta(a)phenanthren-3-yl) acetate
CAS-297-76-7
MFCD00083326
19-Nor-17-alpha-pregn-4-en-20-yne-3-beta,17-diol diacetate
Prestwick0_000908
Prestwick1_000908
Prestwick2_000908
Prestwick3_000908
(3 beta, 17 alpha)-19-Norpregn-4-en-20-yne-3,17 diol Diacetate
SCHEMBL40888
BSPBio_000756
MLS000028661
SPBio_002955
BPBio1_000832
GTPL7072
Ethynodiol diacetate (Standard)
CHEMBL1200624
HY-B1089R
HMS1570F18
HMS2097F18
HMS3714F18
BCP10923
HY-B1089
Tox21_112333
Tox21_112924
BDBM50237627
LMST02030124
s3160
AKOS015895252
Tox21_112333_1
CCG-220908
CS-4640
DB00823
NSC 759288
NCGC00166138-02
NCGC00166138-03
NCGC00166138-04
NCGC00166138-05
AS-13382
SMR000058858
AB00513958
E1315
NS00028774
D01294
ETHYNODIOL DIACETATE COMPONENT OF KELNOR
ETHYNODIOL DIACETATE COMPONENT OF OVULEN
T72249
AB00513958_02
SR-01000872687
Q5405160
SR-01000872687-1
BRD-K46331928-001-05-8
BRD-K46331928-001-06-6
(3beta, 17alpha)-19-Norpregn-4-en-20-yne-3,17-diol diacetate
Ethynodiol diacetate, United States Pharmacopeia (USP) Reference Standard
Solubility of the Compound
The solubility of the compound (3S,8R,9S,10R,13S,14S,17R)-17-acetoxy-17-ethynyl-13-methyl-2,3,6,7,8,9,10,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl acetate can be influenced by several key factors. This compound's complex structure plays a significant role in determining its solubility in various solvents.
Factors Affecting Solubility
In conclusion, the solubility of this compound is likely to be moderate, with a dependency on the solvent chosen. As noted in chemical literature, "the solubility of organic compounds can vary widely and is often best determined experimentally." Thus, understanding the specific interactions in solution will be essential for practical applications.