106036-76-4

Basic information

• Product Name: (+/-) - 3β-hydroxyisopimara-8(14),15-diene
• CAS NO: 106036-76-4
• Molecular Weight: 288.473
• Mol File: 106036-76-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (+/-) - 3β-hydroxyisopimara-8(14),15-diene(CAS DataBase Reference)
• NIST Chemistry Reference: (+/-) - 3β-hydroxyisopimara-8(14),15-diene(106036-76-4)
• EPA Substance Registry System: (+/-) - 3β-hydroxyisopimara-8(14),15-diene(106036-76-4)

Safety Data

• Hazardous Substances Data: 106036-76-4(Hazardous Substances Data)

Upstream product

• 105996-91-6 (+/-) - 3α-t-butyldimethylsilyloxy-13-butylthiomethylene-4α,4β,10α-trimethyl-14 oxo-5β,8α,9β-perhydrophenanthrene 
• 105996-94-9 (+/-) - 3α-t-butyldimethylsilyloxy-13-formyl-4α,4β,10α,13-tetramethyl-1,2,3,4,5β,6,7,9β,10,11,12,13-dodecahydrophenanthrene 
• 105996-93-8 (+/-) - 3α-t-butyldimethylsilyloxy-13-formyl-4α,4β,10α-trimethyl-1,2,3,4,5β,6,7,8α,9β,10,11,12-dodecahydrophenanthrene 
• 105996-90-5 Formic acid (4aR,4bS,8aR,10aR)-7-[1-butylsulfanyl-meth-(Z)-ylidene]-1,1,4a-trimethyl-8-oxo-tetradecahydro-phenanthren-2-yl ester 
• 105996-89-2 (+/-) - 13-butylthiomethylene-3α-hydroxy-4α,4β,10α-trimethyl-14-oxo-5β,8α,9β-perhydrophenanthrene 
• 105996-96-1 tert-Butyl-dimethyl-((2S,4aR,4bS,10aR)-1,1,4a,7-tetramethyl-7-vinyl-1,2,3,4,4a,4b,5,6,7,9,10,10a-dodecahydro-phenanthren-2-yloxy)-silane 

Downstream Products

• 105997-01-1 (S)-3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid (2S,4aR,4bS,7R,10aR)-1,1,4a,7-tetramethyl-7-vinyl-1,2,3,4,4a,4b,5,6,7,9,10,10a-dodecahydro-phenanthren-2-yl ester 
• 105997-00-0 (S)-3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid (2R,4aS,4bR,7S,10aS)-1,1,4a,7-tetramethyl-7-vinyl-1,2,3,4,4a,4b,5,6,7,9,10,10a-dodecahydro-phenanthren-2-yl ester 
• 90044-21-6 oryzalexin B 
• 90044-20-5 oryzalexin C 
• 4728-30-7 sandaracopimaradien-3β-ol 
• 98063-15-1 (+/-)-3β,7α-dihydroxyisopimara-8(14),15-diene 

Relevant articles and documents

SYNTHESIS OF ORYZALEXINS A, B AND C, THE DITERPENOIDAL PHYTOALEXINS ISOLATED FROM RICE BLAST LEAVES INFECTED WITH PYRICULARIA ORIZAE

Naturally occurring enantiomers of three diterpenes isolated as phytoalexins from rice blast leaves were synthesized: (+)-oryzalexin.A (ent-3β-hydroxyisopimara-8(14), 15-dien-7-one,1), (+)-oryzalexin B (ent-7α-hydroxyisopimara-8(14), 15-dien-3-one,2) and (+)-oryzalexin C (ent-isopimara-8(14), 15-diene-3,7-dione, 3).Their antipodes were also synthesized.