79-59-4

Basic information

• Product Name: (1S,αS)-1,2,3,4,4a,7-Hexahydro-1β-hydroxy-α,4aα,8-trimethyl-7-oxonaphthalene-2α-acetic acid
• Synonyms: (1S,αS)-1,2,3,4,4a,7-Hexahydro-1β-hydroxy-α,4aα,8-trimethyl-7-oxonaphthalene-2α-acetic acid;Santoninic acid
• CAS NO: 79-59-4
• Molecular Formula: C₁₅H₂₀O₄
• Molecular Weight: 264.3169
• Mol File: 79-59-4.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (1S,αS)-1,2,3,4,4a,7-Hexahydro-1β-hydroxy-α,4aα,8-trimethyl-7-oxonaphthalene-2α-acetic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,αS)-1,2,3,4,4a,7-Hexahydro-1β-hydroxy-α,4aα,8-trimethyl-7-oxonaphthalene-2α-acetic acid(79-59-4)
• EPA Substance Registry System: (1S,αS)-1,2,3,4,4a,7-Hexahydro-1β-hydroxy-α,4aα,8-trimethyl-7-oxonaphthalene-2α-acetic acid(79-59-4)

Safety Data

• Hazardous Substances Data: 79-59-4(Hazardous Substances Data)

Upstream product

• 481-06-1 α-Santonin 
• 481-06-1 (+/-)-Santonin-D 
• 481-06-1 santonin 

Downstream Products

• 144-62-7 oxalic acid 
• 7732-18-5 water 
• 481-06-1 santonin 
• 64-18-6 formic acid 
• 64-19-7 acetic acid 

Relevant articles and documents

Biology-oriented syntheses (BIOS) of novel santonic-1,3,4-oxadiazole derivatives under microwave-irradiation and their antimicrobial activity

Novel 2-thio substituted 1,3,4-oxadiazole derivatives of santonic acid (13-18) were synthesized. The synthesis of these derivatives was comprised of six steps which start from the basic hydrolysis of á-santonin 1 to the santoninic acid 2 followed by in si

Functionality Transfer from C6 to C8 in Sesquiterpenes. Synthesis of 8-epi-Ivangustin and 8-epi-Isoivangustin from Santonin

The short-range functionality transfer from C6 to C8 in eudesmane framework was reported.Santonin (1) was converted into 8-epi-ivangustin (16) and 8-epi-isoivangustin (18) via synthetic pathway involving the aforementioned functionality transfer and treatment of an intermediate diselenide 9 with m-CPBA.