Название продукции:(2aR,3R,4S,5aS,5bS,7S,7aR,9S,11aR,12aS)-3-((2R,5S)-5-(2-hydroxypropan-2-yl)-2-methyltetrahydrofuran-2-yl)-2a,5a,8,8-tetramethyltetradecahydro-1H,12H-cyclopenta[a]cyclopropa[e]phenanthrene-4,7,9-triol
IUPAC Name:(1S,3R,6S,8R,9S,11S,12S,14S,15R,16R)-15-[(2R,5S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecane-6,9,14-triol
- CAS：78574-94-4
- Молекулярная формула：C30H50O5
- Чистота：97%
- Номер в каталоге：CM133362
- Молекулярная масса：490.73
Только для использования в НИОКР..
Информация о продукции
- Номер CAS:78574-94-4
- Молекулярная формула:C30H50O5
- Точка плавления:-
- Smiles-код:O[C@@H](C1)[C@H]([C@]2(C)O[C@H](C(C)(O)C)CC2)[C@]3(C)[C@]1(C)[C@]4([H])C[C@H](O)[C@@]5([H])C(C)(C)[C@@H](O)CC[C@]56[C@]4(C6)CC3
- Плотность:
- Номер в каталоге:CM133362
- Молекулярная масса:490.73
- Точка кипения:617.2±55.0°C at 760 mmHg
- Номер Mdl:
- Хранение:Store at room temperature.
Category Infos
- Tetrahydrofurans
- Tetrahydrofuran is a heterocyclic organic compound with the molecular formula C4H8O. Tetrahydrofuran belongs to ethers and is the complete hydrogenation product of furan. It is a colorless, water-miscible organic liquid with small viscosity at normal temperature and pressure. Because of its long liquid range, it is a commonly used medium polar aprotic solvent. Its main use is as a precursor of high molecular polymers.
- Steroids
- Naturally occurring steroids are estrogen, cortisol, progesterone, and testosterone. Pharmacologically, they are used in several ways: alter steroid metabolism via statins to help lower cholesterol; as corticosteroids to help control inflammation, asthma, and lupus; and other forms to help hormone deficiency, such as delayed puberty, as well as diseases that result in loss of lean muscle mass, such as cancer and AIDS.
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Column Infos
- Alicyclic Heterocycles
- When the ends of the chains are joined together into a ring, cyclic compounds result; such substances often are referred to as carbocyclic or alicyclic compounds. Substitution of one or more of the ring carbon atoms in the molecules of a carbocyclic compound with a heteroatom gives a heterocyclic compound.
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