105037-83-0

Basic information

• Product Name: 15-hydroxy-7-oxo-abieta-8,11,13-triene
• Synonyms: 15-hydroxy-7-oxo-abieta-8,11,13-triene
• CAS NO: 105037-83-0
• Molecular Formula: C20H28O2
• Molecular Weight: 300.43512
• Mol File: 105037-83-0.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 435.4°Cat760mmHg
• Flash Point: 185.7°C
• Appearance: /
• Density: 1.052g/cm³
• Vapor Pressure: 2.37E-08mmHg at 25°C
• Refractive Index: 1.534
• PKA: 14.43±0.29(Predicted)
• CAS DataBase Reference: 15-hydroxy-7-oxo-abieta-8,11,13-triene(CAS DataBase Reference)
• NIST Chemistry Reference: 15-hydroxy-7-oxo-abieta-8,11,13-triene(105037-83-0)
• EPA Substance Registry System: 15-hydroxy-7-oxo-abieta-8,11,13-triene(105037-83-0)

Safety Data

• Hazardous Substances Data: 105037-83-0(Hazardous Substances Data)

Usage

InChI:InChI=1/C20H28O2/c1-18(2)9-6-10-20(5)15-8-7-13(19(3,4)22)11-14(15)16(21)12-17(18)20/h7-8,11,17,22H,6,9-10,12H2,1-5H3/t17-,20+/m0/s1

Upstream product

• 1239973-47-7 C₂₀H₂₈O₃ 
• 3772-55-2 dehydroabietinol 
• 13601-88-2 dehydroabietinal 
• 1235-74-1 Methyl dehydroabietate 
• 1740-19-8 dehydroabietic acid 
• 75696-40-1 (+)-8,11,13-abietatrien-15-ol 

Relevant articles and documents

AN ABIETANE DITERPENOID FROM SALVIA SAPINAE

Key Word Index - Salvia sapinae; Labiatae; abietane-type diterpenoid; 7β,15-dihydroxy abietatriene.A new abietane-type diterpene, 7β,15-dihydroxyabietatriene, along with three flavonoids, namely apigenin 7,4'-dimethyl ether, genkwanin and cirsimaritin, three triterpenes, including ursolic, oleanolic and 2α,3α-dihydroxyolean-12-en-28-oic acids and sitosterol were isolated from the aerial parts of Salvia sapinae.The structures were elucidated by spectroscopic methods.

Preparation of potential anti-inflammatory agents from dehydroabietic acid

Methyl 16-nor-16-carboxydehydroabietate (22), 16-nor-16- carboxydehydroabietinol acetate (23), methyl 7-keto-16-nor-16- carboxydehydroabietate (29), 16-nor-16-carboxydehydroabietic acid (30), 16- nor-16-carboxydehydroabietinol (31), 7-keto-16-nor-16-carboxydehydroabietic acid (32), methyl 7-hydroxy-16-nor-16-carboxydehydroabietate (33), and 7- hydroxy-16-nor-16-carboxydehydroabietic acid (34) were prepared from dehydroabietic acid. Only 22 and 32 had weak anti-inflammatory activity.