logo
Home  > Chemistry  > Organic Building Blocks  > Alkenyls  > (8S,9S,10R,13R,14S,17R)-17-((R)-6-Hydroxy-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol

AB49960

2140-46-7 | (8S,9S,10R,13R,14S,17R)-17-((R)-6-Hydroxy-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol

Packsize Purity Availability Price Discounted Price    Quantity
5mg 98% in stock $33.00 $23.00 -   +
10mg 98% in stock $58.00 $40.00 -   +
25mg 98% in stock $120.00 $84.00 -   +
100mg 98% in stock $183.00 $128.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Request Bulk Quote
Description
Catalog Number: AB49960
Chemical Name: (8S,9S,10R,13R,14S,17R)-17-((R)-6-Hydroxy-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol
CAS Number: 2140-46-7
Molecular Formula: C27H46O2
Molecular Weight: 402.6529
MDL Number: MFCD00057815
SMILES: O[C@H]1CC[C@]2(C(=CC[C@@H]3[C@@H]2CC[C@]2([C@H]3CC[C@@H]2[C@@H](CCCC(O)(C)C)C)C)C1)C

 

Computed Properties
Complexity: 636  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 8  
Heavy Atom Count: 29  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 5  
XLogP3: 6.8  

 

 

Upstream Synthesis Route 
  • 25-Hydroxycholesterol, also known as 5-cholestene-3β,25-diol, is a key compound utilized in chemical synthesis for various applications. In organic chemistry, 25-Hydroxycholesterol is often employed as a precursor in the synthesis of multiple important molecules, including vitamin D derivatives and steroidal hormones. The presence of a hydroxyl group at the 25th carbon position makes it a valuable intermediate in the production of bioactive compounds that regulate diverse biological processes. Additionally, 25-Hydroxycholesterol serves as a crucial substrate in the development of pharmaceuticals targeting cholesterol metabolism and related pathways. In the realm of medicinal chemistry, its structural versatility enables the creation of analogs with potential therapeutic effects, making it an indispensable component in drug discovery efforts. Furthermore, its use in conjunction with various reagents in synthetic routes allows for the construction of complex molecules with tailored properties, showcasing its significance in advancing chemical synthesis methodologies for scientific and industrial purposes.
Literature
FEATURED PRODUCTS