274251-50-2

Upstream product

• 5419-55-6 Triisopropyl borate 
• 106-38-7 para-bromotoluene 
• 106-44-5 p-cresol 
• 772-80-5 4-methylphenyl chlorosulfate 
• 5720-07-0 4-methoxyphenylboronic acid 

Downstream Products

• 183676-83-7 2-nitro-3-(4-tolyl)thiophene 
• 307301-10-6 7-(4-methylphenyl)-1,2,3,4-tetrahydroisoquinoline 
• 307300-87-4 ethyl 6-(4-methylphenyl)-1H-indole-2-carboxylate 
• 152609-42-2 1-(benzyloxy)-4-ethyl-5-<(6-methyl-6-cyanoheptyl)oxy>-2-(4-methylphenyl)benzene 

Relevant academic research and scientific papers

Synthesis of aryl sulfonamides via palladium-catalyzed chlorosulfonylation of arylboronic acids

A palladium-catalyzed method for the preparation of sulfonamides is described. The process exhibits significant functional group tolerance and allows for the preparation of a number of arylsulfonyl chlorides and sulfonamides under mild conditions.

Tetracyclic compound having lateral halogen substituent and liquid crystal composition comprising the same

A tetracyclic compound expressed by the following general formula (1) wherein H1to H12represent hydrogen atom at least one of which is replaced by a halogen atom, when either H6or H8is replaced by a halogen atom, at least one of the remaining hydrogen atoms is replaced by a halogen atom; R1and Y1independently represent an alkyl group, alkoxy group, or alkoxyalkyl group having 1 to 20 carbon atoms, or an alkenyl group having 2 to 20 carbon atoms, one or more methylene group in R1and Y1may be replaced by oxygen atom, sulfur atom, dihydrosilylene group, dimethylsilylene group, —CH═CH—, or —C≡C—; and X1, X2, and X3independently represent a covalent bond, 1,2-ethylene group, or 1,4-butylene group; and a novel liquid crystal composition comprising the tetracyclic compound and having, at the same time, a wide temperature range of a nematic phase, high optical anisotropy, and high chemical stability.