1219278-10-0

Basic information

• Product Name: BF₄^(1-)*C₂₁H₂₄N₅OS⁽¹⁺⁾
• Synonyms: BF₄^(1-)*C₂₁H₂₄N₅OS⁽¹⁺⁾
• CAS NO: 1219278-10-0
• Molecular Weight: 481.325
• Mol File: 1219278-10-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: BF₄^(1-)*C₂₁H₂₄N₅OS⁽¹⁺⁾(CAS DataBase Reference)
• NIST Chemistry Reference: BF₄^(1-)*C₂₁H₂₄N₅OS⁽¹⁺⁾(1219278-10-0)
• EPA Substance Registry System: BF₄^(1-)*C₂₁H₂₄N₅OS⁽¹⁺⁾(1219278-10-0)

Safety Data

• Hazardous Substances Data: 1219278-10-0(Hazardous Substances Data)

Upstream product

• 623-25-6 p-Xylylene dichloride 
• 61895-53-2 2-(4-chloromethyl-benzyl)-isoindole-1,3-dione 
• 1219277-33-4 BF₄^(1-)*C₁₉H₂₇N₄O₃⁽¹⁺⁾ 
• 1219277-28-7 BF₄^(1-)*C₁₂H₁₆N₃⁽¹⁺⁾ 
• 1219277-23-2 BF₄^(1-)*C₂₀H₁₈N₃O₂⁽¹⁺⁾ 
• 1219277-15-2 C₂₀H₁₈N₃O₂⁽¹⁺⁾*Cl^(1-) 

Downstream Products

• 2010-15-3 3-phenyl-2-thioxoimidazolidin-4-one 

Relevant articles and documents

Traceless approach for the synthesis of 3,5-disubstituted thiohydantoins on functionalized ionic-liquid support

A traceless approach for the synthesis of 3,5-disubstituted thiohydantoins on a novel functionalized ionic-liquid support, 5, is described. Acylation of benzylamine functionalized ionic-liquid support with amino acids yielded ionic-liquid-supported amino acids, which reacted with isothiocyanates to afford ionic-liquid-supported thioureas. Following intramolecular cyclization cleavage from the ionic-liquid support by trifluoroacetic acid (TFA), the desired 3,5-disubstituted thiohydantoins were obtained in good yields and purities. The efficiency of this ionic-liquid-phase strategy facilitated isolation and analysis of intermediates and removal of excess reagents and by-products during the reaction process.