1153358-38-3

Upstream product

• 107-06-2 1,2-dichloro-ethane 
• 86-93-1 1-Phenyl-1H-tetrazole-5-thiol 

Downstream Products

• 1154397-00-8 1-phenyl-5-(vinylsulfonyl)-1H-tetrazole 
• 1156904-86-7 5-((2-chloroethyl)sulfonyl)-1-phenyl-1H-tetrazole 
• 1342313-03-4 (R)-2-methyl-2-phenyl-4-(1-phenyl-1H-tetrazol-5-ylsulfonyl)butanal 
• 1342313-04-5 (R)-2-(4-bromophenyl)-2-methyl-4-(1-phenyl-1H-tetrazol-5-ylsulfonyl)butanal 
• 1342313-05-6 (R)-4-(2-methyl-1-oxo-4-(1-phenyl-1H-tetrazol-5-ylsulfonyl)butan-2-yl)benzonitrile 
• 1342313-06-7 (R)-2-methyl-4-(1-phenyl-1H-tetrazol-5-ylsulfonyl)-2-p-tolylbutanal 
• 1342313-07-8 (R)-2-methyl-2-(naphthalen-2-yl)-4-(1-phenyl-1H-tetrazol-5-ylsulfonyl)butanal 
• 1342313-08-9 (R)-2-(2-fluorophenyl)-2-methyl-4-(1-phenyl-1H-tetrazol-5-ylsulfonyl)butanal 
• 1342313-09-0 (S)-2-methyl-4-(1-phenyl-1H-tetrazol-5-ylsulfonyl)-2-(thiophen-2-yl)butanal 
• 1342313-10-3 (S)-2-methyl-2-propyl-4-(1-phenyl-1H-tetrazol-5-ylsulfonyl)butanal 
• 1342313-11-4 C₁₈H₂₄N₄O₃S 
• 1342313-12-5 (S)-2-benzyl-2-methyl-4-(1-phenyl-1H-tetrazol-5-ylsulfonyl)butanal 
• 1342313-13-6 (R)-2-ethyl-2-phenyl-4-(1-phenyl-1H-tetrazol-5-ylsulfonyl)butanal 
• 1342313-19-2 2-methyl-2-phenyl-4-(1-phenyl-1H-tetrazol-5-ylsulfonyl)butanal 

Relevant academic research and scientific papers

Residual Solvent Signal of CDCl3as a qNMR Internal Standard for Application in Organic Chemistry Laboratory

A nuclear magnetic resonance (NMR) spectrometer is a key instrument in the organic synthesis laboratory for structure determination, reaction control, and compound purity analysis. In addition to qualitative analysis, the application of NMR for quantitati

Enantioselective organocatalytic formal allylation of α-branched aldehydes

Heteroarylvinyl sulfone 1 has been successfully used as a new sulfonyl Michael acceptor in aminocatalytic reactions with branched aldehydes. Subsequent one-pot Julia-Kocienski olefination allows the challenging preparation of enantiomerically pure α-allylated aldehydes bearing C-α quaternary carbons.