28352-34-3

Basic information

• Product Name: (1aS,9bS)-1a,1b,2,3,4,5,5a,9b-octahydrophenanthro[9,10-b]oxirene
• Synonyms: Ccris 7427;Syn-trans-9,10-epoxy-1,2,3,4,4A,9,10,10A-octahydrophenanthrene;Phenanthrene, 9,10-epoxy-1,2,3,4,4A,9,10,10A-octahydro-, syn-trans-;(4Abeta,9beta,10beta)-9,10-epoxy-trans-1,2,3,4,4A,9,10,10A-octahydrophenanthrene
• CAS NO: 28352-34-3
• Molecular Formula: C₁₄H₁₆O
• Molecular Weight: 200.2762
• Mol File: 28352-34-3.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 326.4°C at 760 mmHg
• Flash Point: 146.1°C
• Density: 1.124g/cm³
• Vapor Pressure: 0.000411mmHg at 25°C
• Refractive Index: 1.579
• CAS DataBase Reference: (1aS,9bS)-1a,1b,2,3,4,5,5a,9b-octahydrophenanthro[9,10-b]oxirene(CAS DataBase Reference)
• NIST Chemistry Reference: (1aS,9bS)-1a,1b,2,3,4,5,5a,9b-octahydrophenanthro[9,10-b]oxirene(28352-34-3)
• EPA Substance Registry System: (1aS,9bS)-1a,1b,2,3,4,5,5a,9b-octahydrophenanthro[9,10-b]oxirene(28352-34-3)

Safety Data

• Hazardous Substances Data: 28352-34-3(Hazardous Substances Data)

Upstream product

• 36702-38-2 5,6-dihydro-[1,1'-biphenyl]-2(1H)-one 
• 16804-85-6 8,9-trans-hexahydrophenanthrene 
• 1444-65-1 (RS)-2-phenylcyclohexanone 
• 28352-33-2 9(a)-Hydroxy-10(a)-brom-1,2,3,4,4a,9,10-(trans-4a,10a)-octahydrophenanthren 
• 52092-27-0 trans-(2-phenylcyclohexyl)acetic acid 
• 25662-65-1 trans-1,2,3,4,4a,9,10,10a-octahydrophenanthren-9-ol 
• 21656-46-2 trans-1,2,3,4,4a,10a-hexahydro-9(10H)-phenanthrenone 
• 80738-31-4 <(1S*,2R*)-3-oxo-2-phenylcyclohexyl>acetic acid 

Downstream Products

• 19634-95-8 (+/-)-trans-4b,6,7,8,8a,10-hexahydro-5H-phenanthren-9-one 
• 53446-99-4 (4aR,9S,10S,10aR)-1,2,3,4,4a,9,10,10a-Octahydro-phenanthrene-9,10-diol 
• 53446-96-1 (4aR,9R,10S,10aR)-1,2,3,4,4a,9,10,10a-Octahydro-phenanthrene-9,10-diol 

Relevant articles and documents

Stereoselective Epoxidations and Electrophilic Additions to Partial Ergot Alkaloids and Conformationally-Fixed Styrenes. Experimental and Theoretical Modeling Evidence for the Importance of Torsional Steering as a Stereocontrol Element

Partial ergot alkaloid substrates and related conformationally-fixed styrenes undergo epoxidation, osmium tetraoxide dihydroxylation, and hydrobromination with a level of stereoselectivity which cannot be explained by steric control but is consistent with