79318-19-7

Basic information

• Product Name: Benzoic acid, 4-bromo-, 2-propynyl ester
• CAS NO: 79318-19-7
• Molecular Formula: C10H7BrO2
• Molecular Weight: 239.068
• Mol File: 79318-19-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 4-bromo-, 2-propynyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 4-bromo-, 2-propynyl ester(79318-19-7)
• EPA Substance Registry System: Benzoic acid, 4-bromo-, 2-propynyl ester(79318-19-7)

Safety Data

• Hazardous Substances Data: 79318-19-7(Hazardous Substances Data)

Upstream product

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

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 articles and documents

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

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.

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.