79318-18-6

Basic information

• Product Name: prop-2-yn-1-yl 4-chlorobenzoate
• Synonyms: Benzoic acid, 4-chloro, 2-propynyl ester
• CAS NO: 79318-18-6
• Molecular Formula: C₁₀H₇ClO₂
• Molecular Weight: 194.6144
• Mol File: 79318-18-6.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 292.5°C at 760 mmHg
• Flash Point: 145.3°C
• Density: 1.247g/cm³
• Vapor Pressure: 0.00183mmHg at 25°C
• Refractive Index: 1.554
• CAS DataBase Reference: prop-2-yn-1-yl 4-chlorobenzoate(CAS DataBase Reference)
• NIST Chemistry Reference: prop-2-yn-1-yl 4-chlorobenzoate(79318-18-6)
• EPA Substance Registry System: prop-2-yn-1-yl 4-chlorobenzoate(79318-18-6)

Safety Data

• Hazardous Substances Data: 79318-18-6(Hazardous Substances Data)

Upstream product

• 74-11-3 para-chlorobenzoic acid 
• 122-01-0 4-chloro-benzoyl chloride 
• 107-19-7 propargyl alcohol 
• 106-96-7 propargyl bromide 
• 104-88-1 4-chlorobenzaldehyde 
• 102877-23-6 4-chloro-benzoic acid-(2,3-dibromo-propyl ester) 
• 1236063-61-8 2-bromoallyl 4-chlorobenzoate 

Downstream Products

• 1494702-15-6 (1-benzyl-1H-1,2,3-triazol-4-yl)methyl 4-chlorobenzoate 
• 1494702-50-9 (1-(4-methoxybenzyl)-1H-1,2,3-triazol-4-yl)methyl 4-chlorobenzoate 
• 1494702-52-1 (1-(4-methylbenzyl)-1H-1,2,3-triazol-4-yl)methyl 4-chlorobenzoate 
• 1494702-54-3 (1-(4-(methoxycarbonyl)benzyl)-1H-1,2,3-triazol-4-yl)methyl 4-chlorobenzoate 
• 1494702-56-5 (1-(4-(trifluoromethoxy)benzyl)-1H-1,2,3-triazol-4-yl)methyl 4-chlorobenzoate 
• 1494702-58-7 (1-(4-methoxyphenyl)-1H-1,2,3-triazol-4-yl)methyl 4-chlorobenzoate 
• 1494702-61-2 (1-(p-tolyl)-1H-1,2,3-triazol-4-yl)methyl 4-chlorobenzoate 
• 1494702-64-5 (1-mesityl-1H-1,2,3-triazol-4-yl)methyl 4-chlorobenzoate 
• 1494702-67-8 (1-phenyl-1H-1,2,3-triazol-4-yl)methyl 4-chlorobenzoate 
• 1567324-88-2 (1-(7-chloroquinolin-4-yl)-1H-1,2,3-triazol-4-yl)methyl-4-chlorobenzoate 
• 1428140-66-2 C₁₆H₁₅ClN₆O₂ 
• 1236835-59-8 C₁₇H₁₃Cl₅O₄ 
• 1240483-53-7 1,4,5,6,7,7-hexachlorobicyclo[2.2.1]hepta-2,5-dien-2-ylmethyl 4-chlorobenzoate 

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

Rhodium-catalysed synthesis of fused pyrimidine derivatives employing N-sulfonyl-1,2,3-triazoles as a 1-aza-[4C] synthon

A new synthetic application of N-sulfonyl-1,2,3-triazoles acting as a 1-aza-[4C] synthon via the 1,2-shift reaction of an α-imine rhodium carbene was developed for the synthesis of fused pyrimidine derivatives. The high reactivity of the strained three-me

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