61266-31-7

Upstream product

• 636-98-6 p-nitrobenzene iodide 
• 6089-04-9 3-(tetrahydropyran-2'-yloxy)propyne 

Downstream Products

• 61266-34-0 1-(3-bromoprop-1-yn-1-yl)-4-nitrobenzene 
• 61266-32-8 3-(4-nitrophenyl)prop-2-yn-1-ol 
• 1268381-69-6 (3-(4-nitrophenyl)prop-2-ynyl)(3-phenylprop-2-ynyl)sulfane 
• 1268381-63-0 1-methyl-4-(3-(3-(4-nitrophenyl)prop-2-ynylsulfonyl)prop-1-ynyl)benzene 
• 1268381-68-5 (3-(4-nitrophenyl)prop-2-ynyl)(3-p-tolylprop-2-ynyl)sulfane 
• 1268381-76-5 6-methoxy-4-(4-nitro-phenyl)-1,3-dihydro-naphtho[2,3-c]thiophene 2,2-dioxide 
• 1268381-62-9 1-methoxy-4-(3-(3-(4-nitrophenyl)prop-2-ynylsulfonyl)prop-1-ynyl)benzene 
• 1268381-72-1 C₁₁H₉NO₃S 
• 1268381-67-4 (3-(4-methoxyphenyl)prop-2-ynyl)(3-(4-nitrophenyl)prop-2-ynyl)sulfane 
• 1268381-64-1 1-nitro-4-(3-(3-phenylprop-2-ynylsulfonyl)prop-1-ynyl)benzene 

Relevant academic research and scientific papers

Triazole compounds as well as preparation method and application thereof

The invention belongs to the technical field of medicinal chemistry, and particularly relates to triazole compounds and a preparation method and application thereof. The triazole compounds have excellent LPAR1 antagonistic activity and selectivity, are lo

Selectivity in Garratt-Braverman cyclization: An experimental and computational study

Bispropargyl sulfones equipped with aromatic rings of dissimilar nature were synthesized. Under basic conditions, these sulfones isomerized to the bisallenic sulfones, creating a competitive scenario between two alternate Garratt-Braverman (GB) cyclizatio