59155-84-9

Basic information

• Product Name: METHYL 2-(2-PROPYNYLOXY)BENZENECARBOXYLATE
• Synonyms: METHYL 2-(PROP-2-YN-1-YLOXY)BENZOATE;METHYL 2-(2-PROPYNYLOXY)BENZENECARBOXYLATE
• CAS NO: 59155-84-9
• Molecular Formula: C₁₁H₁₀O₃
• Molecular Weight: 190.2
• Mol File: 59155-84-9.mol
• Article Data: 17

Chemical Properties

• Boiling Point: 100°/0.3mm
• Flash Point: 118.5°C
• Appearance: /
• Density: 1.131g/cm³
• Vapor Pressure: 0.00178mmHg at 25°C
• Refractive Index: 1.528
• CAS DataBase Reference: METHYL 2-(2-PROPYNYLOXY)BENZENECARBOXYLATE(CAS DataBase Reference)
• NIST Chemistry Reference: METHYL 2-(2-PROPYNYLOXY)BENZENECARBOXYLATE(59155-84-9)
• EPA Substance Registry System: METHYL 2-(2-PROPYNYLOXY)BENZENECARBOXYLATE(59155-84-9)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 59155-84-9(Hazardous Substances Data)

Usage

General Description

Methyl 2-(2-propynyloxy)benzenecarboxylate is a chemical compound with the molecular formula C11H10O3. It is a clear, colorless liquid that is insoluble in water but soluble in organic solvents. METHYL 2-(2-PROPYNYLOXY)BENZENECARBOXYLATE is commonly used in the synthesis of pharmaceuticals and agrochemicals. It is also utilized in the production of fragrances and flavorings. The propynyloxy group in the molecule makes it highly reactive and useful in various organic reactions. However, it is important to handle this compound with care as it can be potentially hazardous if not used properly.

InChI:InChI=1/C11H10O3/c1-3-8-14-10-7-5-4-6-9(10)11(12)13-2/h1,4-7H,8H2,2H3

Upstream product

• 69-72-7 salicylic acid 
• 106-96-7 propargyl bromide 
• 119-36-8 methyl salicylate 

Downstream Products

• 55582-31-5 2-(prop-2-yn-1-yloxy)benzoic acid 
• 119-36-8 methyl salicylate 
• 267890-16-4 2-[3'-(2-Thienyl)prop-2'-ynyloxy]benzoic acid 
• 267890-12-0 2-[(3’-phenyl)prop-2’-ynyloxy]benzoic acid 
• 267890-13-1 2-[3'-(o-Methoxyphenyl)prop-2'-ynyloxy]benzoic acid 
• 267890-20-0 2-[3'-(o-Iodophenyl)prop-2'-ynyloxy]benzoic acid 
• 267890-15-3 2-[3'-(o-Methoxycarbonylphenyl)prop-2'-ynyloxy]benzoic acid 
• 267890-17-5 2-[3'-(o-Acetoxyphenyl)prop-2'-ynyloxy]benzoic acid 
• 267890-19-7 2-[3'-(2,4-Dimethoxypyrimidin-5-yl)prop-2'-ynyloxy]benzoic acid 
• 65211-53-2 2-Prop-2-ynyloxybenzoic acid chloride 
• 230955-92-7 Methyl (2R,4R)-2-phenyl-3-<2-(prop-2-ynyloxybenzoyl)>hiazolidine-4-carboxylate 
• 230955-95-0 (2R,4R)-2-Phenyl-3-<2-(prop-2-ynyloxybenzoyl)>thiazolidine-4-carboxylic acid 
• 1334526-86-1 methyl 2-(buta-2,3-dienyloxy)benzoate 
• 1404189-16-7 C₂₀H₁₄BrN₃O₅ 

Relevant articles and documents

Design and synthesis of triazole conjugated novel 2,5-diaryl substituted 1,3,4-oxadiazoles as potential antimicrobial and anti-fungal agents

A series of triazole conjugated novel 2,5-diaryl 1,3,4-oxadiazole derivatives 8a-q are efficiently synthesized starting from methyl salicylate. All the synthesized compounds were characterized based on their 1H NMR, 13C NMR, Mass and

Synthesis, in silico Pharmacokinetic and Antimicrobial Studies of Oxovanadium(V) Complexes with 2-(4-((2-(Carboxy)phenoxy) methyl)-1H-1,2,3-triazol-1-Yl)Benzoic Acid

New Vanadium(V) complexes with new ligand 2-(4-((2-(carboxy) phenoxy) methyl)-1H-1,2,3triazol-1-yl)benzoic acid (L1) has been synthesized and characterized by different analytical techniques such as elemental analyzer, 1H NMR, UV-Vis

Gold promoted arylative cyclization of alkynoic acids with arenediazonium salts

Alkynoic acids derived from salicylic acid and analogues undergo arylative cyclization with arenediazonium salts promoted by gold in the absence of external ligands. The reaction is thermally induced and proceeds even in the absence of light. A difference in regioselectivity has been found compared with that observed in the cycloisomerization process of the same type of compounds.