19123-29-6

Basic information

• Product Name: 3-Ethenyldodecahydro-3,4a,7,7,10a-pentamethyl-1H-naphtho[2,1-b]pyran
• Synonyms: 3-Ethenyldodecahydro-3,4a,7,7,10a-pentamethyl-1H-naphtho[2,1-b]pyran;3-ethenyl-3,4a,7,7,10a-pentamethyldodecahydro-1H-benzo[f]chromene
• CAS NO: 19123-29-6
• Molecular Formula: C₂₀H₃₄O
• Molecular Weight: 290.48
• Mol File: 19123-29-6.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-Ethenyldodecahydro-3,4a,7,7,10a-pentamethyl-1H-naphtho[2,1-b]pyran(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Ethenyldodecahydro-3,4a,7,7,10a-pentamethyl-1H-naphtho[2,1-b]pyran(19123-29-6)
• EPA Substance Registry System: 3-Ethenyldodecahydro-3,4a,7,7,10a-pentamethyl-1H-naphtho[2,1-b]pyran(19123-29-6)

Safety Data

• Hazardous Substances Data: 19123-29-6(Hazardous Substances Data)

Upstream product

• 596-85-0 epimanool 

Relevant articles and documents

Microbial Transformation of Manool and (12Z)-Labda-8(17),12,14-triene by Rhodococcus erythropolis JTS-131

Rhodococcus erythropolis JTS-131, a cis-abienol and sclareol transformable bacterium, converted manool and accumulated manoyl oxide in the culture broth.In the presence of metabolic inhibitors, 13β-hydroxylabda-8(17),14-dien-18-oic acid and its methylester (a new compound) were accumulated as the transformation products.This strain also transformed (12Z)-labda-8(17),12,14-triene and accumulated (12Z)-labda-8(17),12,14-trien-18-al in the culture broth.In the presence of metabolic inhibitors, two compounds, (12Z)-labda-8(17),12,14-trien-18-ol and 4,18,19-trinor-3,4-seco-5-oxo-(12Z)-labda-8(17),12,14-trien-3-oic acid were accumulated.Based on the experiments on the degradation sequence, transformation pathways for these two labdanes by the bacterium are proposed.