233751-73-0

Basic information

• Product Name: 10-phenylseleno-2-pinene
• Synonyms: 10-phenylseleno-2-pinene
• CAS NO: 233751-73-0
• Molecular Weight: 291.295
• Mol File: 233751-73-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 10-phenylseleno-2-pinene(CAS DataBase Reference)
• NIST Chemistry Reference: 10-phenylseleno-2-pinene(233751-73-0)
• EPA Substance Registry System: 10-phenylseleno-2-pinene(233751-73-0)

Safety Data

• Hazardous Substances Data: 233751-73-0(Hazardous Substances Data)

Upstream product

• 68395-72-2 N-phenylselenenyl succinimide 
• 18172-67-3 beta-pinene 
• 253426-88-9 Pinocarveylchlorid 
• 23974-72-3 sodium phenylselenide 
• 19894-97-4 (1R)-Myrtenol 
• 1666-13-3 diphenyl diselenide 
• 55527-89-4 (-)-myrtenyl bromide 

Downstream Products

• 19894-98-5 6,6-dimethyl-2-methylene-bicyclo[3.1.1]heptan-3-ol 
• 233751-80-9 C₄₈H₇₉NO₇SSi₂ 
• 233751-84-3 1-[2-(tert-Butyl-dimethyl-silanyloxy)-3-((1R,5S,6S,8R)-9,9-dimethyl-4,4-dioxo-4λ⁶-thia-tricyclo[6.1.1.0^2,6]dec-2-en-5-yl)-4,6-dimethoxy-phenyl]-3-methyl-butan-1-one 
• 233751-83-2 1-{2-(tert-Butyl-dimethyl-silanyloxy)-3-[(S)-((1R,3S,5R)-6,6-dimethyl-2-methylene-bicyclo[3.1.1]hept-3-yl)-hydroxy-methyl]-4,6-dimethoxy-phenyl}-3-methyl-butan-1-one 
• 233751-74-1 C₂₈H₄₇NO₂SSi 

Relevant articles and documents

Syntheses of the optically active terpene hydroxyphenylselenides

The optically active hydroxyphenylselenides derived from the p-menthane, carane, and pinane systems have been obtained. Two methods of hydroxyphenylselenides synthesis have been compared. The first method is based on the reaction of alkenes with N-(phenylseleno)succinimide in the presence of water, and the second from epoxides as a result of the reaction with sodium benzeneselenolate. The influence of the substrate structures on the composition of the obtained products has been demonstrated.

Metallated 2-alkenyl sulfoximines in asymmetric synthesis: Regio- and stereoselective synthesis of highly substituted oxabicyclic ethers and studies towards the total syntheses of the euglobals G1 and G2 and arenaran A

2-Cyclopentenyl- and 2-cyclohexenylmethyl sulfoximines can be converted into angular carbon-functionalised, highly substituted, isomerically pure (ds ± 98%) 2-oxabicyclo[3.3.0]octanes and 2-oxabicyclo[3.4.0]nonanes in high yields by a convenient one-pot sequence. Molecular frameworks such as these can be found in many biologically active natural products. In addition to the methodological work, we report on studies towards the total synthesis of the euglobals G1 and G2 and arenaran A.