84848-19-1

Basic information

• Product Name: (8alpha)-6'-methoxycinchonan-9(R)-ol mono[(1S)-7,7-dimethyl-2-oxobicyclo[2.2.1]heptane-1-methanesulphonate]
• Synonyms: (8alpha)-6'-methoxycinchonan-9(R)-ol mono[(1S)-7,7-dimethyl-2-oxobicyclo[2.2.1]heptane-1-methanesulphonate];(8alpha)-6'-Methoxycinchonan-9(R)-ol mono((1S)-7,7-dimethyl-2-oxobicyclo(2.2.1)heptane-1-methanesulphonate);Einecs 284-305-6
• CAS NO: 84848-19-1
• Molecular Formula: 2C₁₀H₁₆O₄S*C₂₀H₂₄N₂O₂
• Molecular Weight: 556.7134
• EINECS: 284-305-6
• Mol File: 84848-19-1.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (8alpha)-6'-methoxycinchonan-9(R)-ol mono[(1S)-7,7-dimethyl-2-oxobicyclo[2.2.1]heptane-1-methanesulphonate](CAS DataBase Reference)
• NIST Chemistry Reference: (8alpha)-6'-methoxycinchonan-9(R)-ol mono[(1S)-7,7-dimethyl-2-oxobicyclo[2.2.1]heptane-1-methanesulphonate](84848-19-1)
• EPA Substance Registry System: (8alpha)-6'-methoxycinchonan-9(R)-ol mono[(1S)-7,7-dimethyl-2-oxobicyclo[2.2.1]heptane-1-methanesulphonate](84848-19-1)

Safety Data

• Hazardous Substances Data: 84848-19-1(Hazardous Substances Data)

Usage

General Description

The chemical "(8alpha)-6'-methoxycinchonan-9(R)-ol mono[(1S)-7,7-dimethyl-2-oxobicyclo[2.2.1]heptane-1-methanesulphonate]" is a compound that consists of cinchonan-9(R)-ol and (1S)-7,7-dimethyl-2-oxobicyclo[2.2.1]heptane-1-methanesulphonate. Cinchonan-9(R)-ol is a derivative of cinchona alkaloids, which are commonly used as chiral ligands in asymmetric synthesis. The addition of (1S)-7,7-dimethyl-2-oxobicyclo[2.2.1]heptane-1-methanesulphonate acts as a protecting group, preventing unwanted reactions and allowing for selective modification of the compound. This chemical compound may have applications in organic synthesis, pharmaceuticals, and other fields where chiral molecules are important.

Upstream product

• 3144-16-9 (1S)-10-camphorsulfonic acid 
• 130-95-0 Quinine 

Relevant articles and documents

Multiple-responsive ionic complex luminogen of quinine and camphorsulfonic acid with aggregation-induced emission

Bulky camphorsulfonic acid (CSA) was used to complex with quinine (Qu) to impose restricted intramolecular rotation (RIR) required for aggregation-induced emission (AIE) properties. After complexation with two equivalents of CSA, the non-emissive quinine (Qu) base can be protonated to produce an ionic complex Qu(CSA)2 with AIE properties. The ionic bonds in the complex Qu(CSA)2 are sensitive to various external stimuli, which allows its use as a luminescent sensor for pH values and different metal ions. Moreover, the ionic Qu(CSA)2 can be a denaturant and biological sensor for the blood protein of bovine serum albumin (BSA); through the use of Qu(CSA)2, the unfolding process of the BSA chains was evaluated. Theoretical and practical aspects of this ionic Qu(CSA)2 complex are discussed in this study.