1393596-52-5

Basic information

• Product Name: C₁₀₂H₉₆N₁₈O₂₄
• CAS NO: 1393596-52-5
• Molecular Weight: 1957.99
• Mol File: 1393596-52-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₁₀₂H₉₆N₁₈O₂₄(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₀₂H₉₆N₁₈O₂₄(1393596-52-5)
• EPA Substance Registry System: C₁₀₂H₉₆N₁₈O₂₄(1393596-52-5)

Safety Data

• Hazardous Substances Data: 1393596-52-5(Hazardous Substances Data)

Upstream product

• 1393596-06-9 C₃₀H₂₉N₅O₇ 
• 15911-93-0 2,4,6-tris-prop-2-ynyloxy-[1,3,5]triazine 

Relevant articles and documents

Regio- and diastereoselective synthesis of β-lactam-triazole hybrids via passerini/CuAAC sequence

Passerini (P-3CR) and Passerini-Smiles reactions were investigated in azetidine-2,3-diones, affording the corresponding 3,3-disubstituted-β- lactams with complete diastereoselectivity in high yields. The study has been carried out using different isocyanides, carboxylic acids, and phenols showing the scope of both reactions. In addition, the regioselective synthesis of highly functionalized β-lactam-triazole hybrids has been developed via a Passerini/CuAAC sequence. Interestingly, the use of dialkynes/diazides or trialkynes/triazides as linkers in the CuAAC step has allowed the synthesis of C2 and C3 symmetric β-lactam-triazole hybrids, respectively.