169176-73-2

Basic information

• Product Name: (S)-4-hydroxysattabacin
• Synonyms: (S)-4-hydroxysattabacin
• CAS NO: 169176-73-2
• Molecular Weight: 222.284
• Mol File: 169176-73-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (S)-4-hydroxysattabacin(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-4-hydroxysattabacin(169176-73-2)
• EPA Substance Registry System: (S)-4-hydroxysattabacin(169176-73-2)

Safety Data

• Hazardous Substances Data: 169176-73-2(Hazardous Substances Data)

Upstream product

• 5674-02-2 2-methylpropylmagnesium chloride 
• 915396-55-3 (S)-2-hydroxy-3-(4-hydroxyphenyl)-N-methoxy-N-methylpropanamide 
• 920-36-5 (2-methylpropyl)lithium 
• 1236191-26-6 (S)-3-(O-tert-butyldimethylsiloxy)-4-O-tert-butyldimethylsiloxysattabacin 

Downstream Products

• 1236191-27-7 (S)-4-acetoxy-8-acetylsattabacin 

Relevant articles and documents

Synthesis of Weinreb amides using diboronic acid anhydride-catalyzed dehydrative amidation of carboxylic acids

The first successful example of the direct synthesis of Weinreb amides using catalytic hydroxy-directed dehydrative amidation of carboxylic acids using the diboronic acid anhydride catalyst is described. The methodology is applicable to the concise syntheses of eight α-hydroxyketone natural products, namely, sattabacin, 4-hydroxy sattabacin, kurasoins A and B, soraphinols A and B, and circumcins B and C.

Discovery and total synthesis of a new estrogen receptor heterodimerizing actinopolymorphol A from actinopolymorpha rutilus

(Equation Presented). Estrogen receptor ERα and ERβ heterodimerization has been implicated in cancer chemoprevention. The discovery, structural elucidation, and total synthesis of a new natural product, actinopolymorphol A (1), from Actinopolymorpha rutil