- A Firefox/Tampermonkey userscript was prototyped that shows a 2-D chemical structure (rendered with SMILES-drawer.js) in a tooltip whenever the user hovers over a recognized chemical name on any web page; the dictionary of names and SMILES strings is currently hard-coded but could be extended dynamically.  
- Discussion of an “organic-chemistry student app” that photographs hand-drawn structural formulas and returns the correct IUPAC name or SMILES string; the open-source tool Imago (OCR for chemical diagrams) and the newer ML model MolScribe (paper: arXiv 2205.14311, demo on Hugging Face) were identified as existing solutions, with MolScribe already achieving high accuracy on neat hand-drawn molecules.  
- Participants debated packaging such an app: Electron was proposed as the quickest cross-platform wrapper despite its bloat, while alternatives such as native Swift/Kotlin or lighter JS frameworks were considered slower to ship and harder to maintain.  
- EU retinol concentration limits (0.3 % for face creams, 0.05 % for body lotions) were noted as a recent regulatory change affecting consumer skincare formulations.  
- A speculative medical-cooling concept was explored: micro-encapsulated endothermic decomposition reactions (borohydrides, azides) or conformational phase changes in aligned polymers/rotaxanes could act as perfusable heat sinks for suspended animation, provided activation energy, toxicity, and gas-product management are solved.