103215-02-7

Basic information

• Product Name: C₃₁H₃₂O₉S₂
• CAS NO: 103215-02-7
• Molecular Weight: 612.722
• Mol File: 103215-02-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₃₁H₃₂O₉S₂(CAS DataBase Reference)
• NIST Chemistry Reference: C₃₁H₃₂O₉S₂(103215-02-7)
• EPA Substance Registry System: C₃₁H₃₂O₉S₂(103215-02-7)

Safety Data

• Hazardous Substances Data: 103215-02-7(Hazardous Substances Data)

Upstream product

• 87-66-1 2-hydroxyresorcinol 
• 100-44-7 benzyl chloride 
• 103215-00-5 4-(benzyloxy)-2-ethoxybenzo[d][1,3]dioxole 
• 52800-47-2 3-(benzyloxy)benzene-1,2-diol 
• 103214-99-9 2-ethoxy4-hydroxy-1,3-benzodioxol 
• 103215-01-6 1-Benzyloxy-2,3-bis<2-hydroxyethoxy>benzol 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 103215-07-2 syn-o,o'-Dibenzyloxy-dibenzo<18>krone-6 
• 103215-19-6 anti-o,o'-Dibenzyloxy-dibenzo<18>krone-6 

Relevant articles and documents

Chinone von Benzo- und Dibenzokronenethern

The preparation of the 1,4-quinones of benzocrown-5 (1), benzocrown-6 (2), and dibenzocrown-6 (3) and their quinols is described.The quinones are obtained by Fremy salt oxidation of the corresponding 3-hydroxybenzo-crown ethers which are readily accessible by a double protective group synthesis from 1,2,3-trihydroxybenzene.The synthetic pathway also provides a general high yield preparation of 2,3-dialkoxy-1,4-benzoquinones.The new crown ethers are characterised by 1H- and 13C-N.M.R. as well as U.V. spectroscopy.Non-aqueous redox potentials aredetermined by cyclic voltammetry.Crystalline complexes of 1 and 2 with various ammonium, alkali, and alkaline earth cations are also described.