79318-19-7

Upstream product

• 107-19-7 propargyl alcohol 
• 1122-91-4 4-bromo-benzaldehyde 
• 586-76-5 4-Bromobenzoic acid 
• 586-75-4 4-chlorobenzoyl chloride 
• 106-96-7 propargyl bromide 

Downstream Products

• 130444-11-0 4-Bromo-benzoic acid 4-dihexylamino-but-2-ynyl ester 
• 130421-66-8 4-Bromo-benzoic acid 4-dioctylamino-but-2-ynyl ester 
• 1240483-54-8 1,4,5,6,7,7-hexachlorobicyclo[2.2.1]hepta-2,5-dien-2-ylmethyl 4-bromobenzoate 
• 1494702-22-5 (1-benzyl-1H-1,2,3-triazol-4-yl)methyl 4-bromobenzoate 
• 1236835-60-1 C₁₇H₁₃BrCl₄O₄ 
• 130421-64-6 4-Bromo-benzoic acid 4-diethylamino-but-2-ynyl ester 
• 130421-63-5 4-Bromo-benzoic acid 4-dimethylamino-but-2-ynyl ester 
• 130421-65-7 4-Bromo-benzoic acid 4-dibutylamino-but-2-ynyl ester 

Relevant academic research and scientific papers

Regioselective synthesis, antibacterial, and antioxidant activities of ester-linked 1,4-disubstituted 1,2,3-triazoles

Abstract: Synthesis of ester-linked 1,4-disubstituted 1,2,3-triazoles was carried out in water through cycloaddition between benzoic acid prop-2-yn-1-yl esters and aromatic azides using cellulose-supported cuprous iodide nanoparticles. Structures of all t

Combining oxidative N-heterocyclic carbene catalysis with click chemistry: A facile one-pot approach to 1,2,3-triazole derivatives

A combination of the oxidative N-heterocyclic carbene catalysis and click chemistry has been explored for the direct, one-pot synthesis of 1,2,3-triazole derivatives from aromatic aldehydes. This procedure was found to be very efficient and a variety of 1

Synthesis of para-substituted 1,4,5,6,7,7-hexachlorobicyclo-[2.2.1]hepta-2, 5-dien-2-ylmethyl benzoates

[4 + 2]-Cycloaddition of hexachlorocyclopentadiene to para-substituted prop-2-yn-1-yl benzoates gave the corresponding 1,4,5,6,7,7-hexachlorobicyclo[2. 2.1]hepta-2,5-dien-2-ylmethyl benzoates. The structure of the adducts was confirmed by independent synthesis, esterification of para-substituted benzoic acids with 1,4,5,6,7,7-hexachlorobicyclo[2.2.1]hepta-2,5-dien-2-ylmethanol.

Synthesis of 1,4,5,6-tetrachloro-7,7-dimethoxybicyclo[2.2.1]hepta-2,5- dienylmethyl esters of p-substituted benzoic acids

The possibility of preparing 1,4,5,6-tetrachloro-7,7-dimethoxybicyclo[2.2. 1]hepta-2,5-dienyl-methyl esters of p-substituted benzoic acids by [4+2]cycloaddition of tetrachlorodimethoxycyclo-pentadine to propargyl esters of the corresponding acids was exam

A facile direct conversion of aldehydes to esters and amides using acetone cyanohydrin

Aromatic aldehydes with electron-withdrawing groups undergo rapid reactions with a variety of alcohols and secondary amines to afford the corresponding esters and amides, respectively, in high yields, when treated with NaCN or acetone cyanohydrin and base under ambient reaction conditions. In case of α,β-unsaturated aldehydes, simultaneous reduction of the CC bond along with esterification occurred to produce the saturated esters in high yields.