(11beta,16alpha)-11,16,17-Trihydroxy-3,20-dioxopregna-1,4-dien-21-yl acetate(CAS: 86401-80-1)

CAS Number
Related Products
2-Phenyl-9,10-anthraquinone
CAS Number: 6485-97-8
1,7-Dichloroisoquinoline
CAS Number: 70810-24-1
Silane, chloromethyloctadecyl-
CAS Number: 124694-97-9
2,4,5-Triphenyl-1H-imidazole
CAS Number: 484-47-9
Other Suppliers for (11beta,16alpha)-11,16,17-Trihydroxy-3,20-dioxopregna-1,4-dien-21-yl acetate
Basic Information
Molecular Formula
C23H30O7
Molecular Weight
418.49 g/mol
Physical Properties
Boiling Point
593.3°C at 760 mmHg
Density
1.34
Flash Point
202.5°C
Chemical Identifiers
SMILES
CC(=O)OCC(=O)[C@]1([C@@H](C[C@@H]2[C@@]1(C[C@@H]([C@H]3[C@H]2CCC4=CC(=O)C=C[C@]34C)O)C)O)O
InChIKey
AAMGSJIEPUHTOK-GIMXSRRZSA-N
Database References
MDL Number
MFCD08460167
FAQ
(11beta,16alpha)-11,16,17-Trihydroxy-3,20-dioxopregna-1,4-dien-21-yl acetate is an organic compound with a molecular weight of approximately 426.45 g/mol. It has a crystalline form at room temperature and is poorly soluble in water. The compound exhibits a high reactivity due to the presence of hydroxyl and carbonyl groups, making it susceptible to hydrolysis and oxidation. It is stable under anhydrous and neutral conditions but should be stored under conditions that minimize moisture and oxygen exposure.
(11beta,16alpha)-11,16,17-Trihydroxy-3,20-dioxopregna-1,4-dien-21-yl acetate is typically synthesized through a multi-step process involving the conversion of progesterone to the target compound. The reaction involves acetylation and subsequent hydroxylation steps, with careful control of reaction conditions to achieve high yields and selectivity. Commonly used catalysts include acid catalysts and enzymes, and the process is optimized for efficiency and environmental friendliness.
(11beta,16alpha)-11,16,17-Trihydroxy-3,20-dioxopregna-1,4-dien-21-yl acetate is primarily used in the pharmaceutical industry for the synthesis of progestogens and other steroid compounds. It is also of interest in research and development for its potential applications in biomedical sensors and semiconductors. Its use in polymer science for the development of novel biomaterials is also under investigation.
When handling (11beta,16alpha)-11,16,17-Trihydroxy-3,20-dioxopregna-1,4-dien-21-yl acetate, it is essential to wear appropriate personal protective equipment (PPE) such as gloves and safety goggles. The compound should be handled in a well-ventilated area or under a fume hood to minimize exposure. Spills should be cleaned up immediately using appropriate absorbents, and the area should be flushed with water. A safety data sheet (SDS) should be consulted for detailed handling and emergency procedures. Storage should be in a cool, dry place away from moisture and heat sources.
Safety Notice
Please verify product specifications and safety data before use. Contact the supplier for detailed safety information.
Always follow proper handling procedures
Contact Information
Contact Person
Li Jun
2801519207@qq.com








![[4-(Difluoromethoxy)phenyl]acetonitrile](https://static.chemtradehub.com/structs/414/41429-16-7-ae43.webp)



