41216-85-7

Basic information

• Product Name: dimethyl bicyclo[2.2.2]oct-2-ene-2,3-dicarboxylate
• Synonyms: dimethyl bicyclo[2.2.2]oct-2-ene-2,3-dicarboxylate
• CAS NO: 41216-85-7
• Molecular Formula: C12H16O4
• Molecular Weight: 224.25304
• Mol File: 41216-85-7.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: dimethyl bicyclo[2.2.2]oct-2-ene-2,3-dicarboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: dimethyl bicyclo[2.2.2]oct-2-ene-2,3-dicarboxylate(41216-85-7)
• EPA Substance Registry System: dimethyl bicyclo[2.2.2]oct-2-ene-2,3-dicarboxylate(41216-85-7)

Safety Data

• Hazardous Substances Data: 41216-85-7(Hazardous Substances Data)

Upstream product

• 1165952-91-9 cyclohexa-1,3-diene 
• 762-42-5 dimethyl acetylenedicarboxylate 
• 950-65-2 dimethyl bicyclo[2.2.2]octa-2,5-diene-2,3-dicarboxylate 

Downstream Products

• 151813-29-5 Bicyclo<2.2.2>oct-2-ene-2,3-dicarboxylic anhydride 
• 202823-67-4 3,6-dichloro-4,5-diazatricyclo[6.2.2.2,7]dodeca-2⁽⁷⁾,3,5-triene 
• 1560642-62-7 C₂₈H₃₂ClN₅O₂ 
• 1560642-66-1 C₄₄H₅₂N₈O₄ 
• 1560649-14-0 C₄₈H₅₈N₁₀O₆ 
• 7399-31-7 Bicyclo<2.2.2>oct-2-ene-2,3-dinitril 

Relevant articles and documents

Bridged Ring compounds As Hepatitis C Virus (HCV) Inhibitors And Pharmaceutical Applications Thereof

Provided herein is a compound having Formula (I), or a stereoisomer, a geometric isomer, a tautomer, an N-oxide, a hydrate, a solvate, a metabolite, a pharmaceutically acceptable salt or a prodrug thereof, which can be used for treating HCV infection or a HCV disorder. Also provided herein are pharmaceutical compositions comprising the compounds disclosed herein, which can be used for treating HCV infection or a HCV disorder.

Photochemical reactions of charge-transfer complexes. IV. The orientation effects of charge-transfer complexes: theory and experiment

In paper number III of this series (2) ab initio and PCILO molecular orbital calculations for the four ?-?* charge-transfer (ct) complexes formed between maleonitrile (MN) and fumaronitrile (FN), and cis (CS) and trans-1,2-dimethoxyethylene (TR) were reported.This paper reports the ct transition absorption characteristics and association constans of these complexes as a function of temperature.From this data the heats of formation of the complexes are determined and these experimental results are then compared with the theoretical values; good agreement is obtained.The order of complex stability ( (kcal mol)) measured in chloroform solution is: MN-TR(0.55) FN-TR(0.65) MN-CS(0.78) FN-CS(1.25) we reach the conclusion that for these complexes orientation effects of the substituents are quite small in magnitude and that the dominant factor influencing complex stability follows the redox potential difference.The structures of the complexes are discussed in view of these results.