17275-82-0

Basic information

• Product Name: ETHYL 3,5-DIMETHOXYBENZOATE
• Synonyms: RARECHEM AL BI 0065;ETHYL 3,5-DIMETHOXYBENZOATE;3,5-DIMETHOXYBENZOIC ACID ETHYL ESTER;Einecs 241-308-7
• CAS NO: 17275-82-0
• Molecular Formula: C₁₁H₁₄O₄
• Molecular Weight: 210.23
• EINECS: 241-308-7
• Product Categories: Aromatic Esters
• Mol File: 17275-82-0.mol
• Article Data: 25

Chemical Properties

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Appearance: /
• Density: g/cm³
• Vapor Pressure: 0.00288mmHg at 25°C
• Refractive Index: 1.495
• CAS DataBase Reference: ETHYL 3,5-DIMETHOXYBENZOATE(CAS DataBase Reference)
• NIST Chemistry Reference: ETHYL 3,5-DIMETHOXYBENZOATE(17275-82-0)
• EPA Substance Registry System: ETHYL 3,5-DIMETHOXYBENZOATE(17275-82-0)

Safety Data

• Hazardous Substances Data: 17275-82-0(Hazardous Substances Data)

Usage

InChI:InChI=1/C11H14O4/c1-4-15-11(12)8-5-9(13-2)7-10(6-8)14-3/h5-7H,4H2,1-3H3

Upstream product

• 4142-98-7 ethyl 3,5-dihydroxybenzoate 
• 74-88-4 methyl iodide 
• 64-17-5 ethanol 
• 1132-21-4 3,5-dimethoxybenzoic acid 
• 99-10-5 3,5-Dihydroxybenzoic acid 
• 7311-34-4 3,5-dimethoxybenzaldehdye 
• 60-29-7 diethyl ether 
• 17213-57-9 3,5-dimethoxybenzoyl chloride 
• 71-43-2 benzene 
• 108-46-3 recorcinol 
• 2150-37-0 methyl 3,5-dimethoxybenzoate 
• 7051-16-3 1-chloro-3,5-dimethoxybenzene 
• 95-92-1 oxalic acid diethyl ester 
• 6148-64-7 ethyl potassium malonate 

Downstream Products

• 17275-83-1 3,5-dimethoxy-2-nitro-benzoic acid ethyl ester 
• 51707-38-1 3,5-dimethoxy-benzoic acid hydrazide 
• 77376-80-8 α-methylsulphinyl-3,5-dimethoxyacetophenone 
• 39507-96-5 3,5-dimethoxy-α,α-dimethyl benzyl alcohol 
• 500-49-2 5-propyl-1,3-benzenediol 
• 22976-40-5 1,3-dimethoxy-5-pentylbenzene 
• 500-67-4 spherophorol 
• 41395-10-2 1,3-dimethoxy-5-propylbenzene 
• 3158-56-3 5-n-pentadecylresorcinol 
• 23032-48-6 1,3-dimethoxy-5-pentadecylbenzene 
• 6121-64-8 5-n-heptyl resorcinol dimethyl ether 
• 17213-58-0 3,5-dimethoxybenzamide 
• 4299-73-4 6-ethyl-2,4-dihydroxybenzoic acid 
• 3686-57-5 2,4-dimethoxy-6-methylbenzoic acid 

Relevant articles and documents

Nickel-Catalyzed Esterification of Amides Under Mild Conditions

Abstract: The use of ligands to adjust the catalytic activity of the catalyst for esterification of amides is challenge in organic chemistry. In this paper, Nickel(II)-NHC-catalyzed the esterification reaction between N,N-di-Boc amide and alcohols at room temperature have been demonstrated. The imidazolium salt bearing a hydroxyl functionalized side arm showed high effective catalytic activity in the activation of the amide N–C bond in air atmosphere. Graphic Abstract: [Figure not available: see fulltext.].

Facile, highly efficient and environmentally friendly transesterification mediated by platinum dioxide and nickel oxide under essentially neutral conditions

A practical, facile and highly efficient transesterification reaction under essentially neutral conditions was achieved using platinum dioxide (PtO2) or PtO2/nickel oxide (NiO) as the catalyst. A number of esters and alcohols that contain various functional groups were employed. Good to excellent yields were obtained for different aromatic or aliphatic starting materials. The Pt-alcohol intermediate generated in situ facilitated the exchange of low-alcohol esters to high-alcohol esters.

Diethyloxalate as “CO” Source for Palladium-Catalyzed Ethoxycarbonylation of Bromo- and Chloroarene Derivatives

Palladium(II)-catalyzed ethoxycarbonylation of aryl bromides with diethyloxalate oxalate is described. Functionalized aromatic esters can be efficiently synthesized with only 0.65 mol % PdCl2(PPh3)2 catalyst under microwav