704913-84-8

Basic information

• Product Name: 2-Furancarboxylicacid,3-ethyl-,methylester(9CI)
• Synonyms: 2-Furancarboxylicacid,3-ethyl-,methylester(9CI)
• CAS NO: 704913-84-8
• Molecular Formula: C₈H₁₀O₃
• Molecular Weight: 0
• Product Categories: CARBOXYLICESTER
• Mol File: 704913-84-8.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-Furancarboxylicacid,3-ethyl-,methylester(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Furancarboxylicacid,3-ethyl-,methylester(9CI)(704913-84-8)
• EPA Substance Registry System: 2-Furancarboxylicacid,3-ethyl-,methylester(9CI)(704913-84-8)

Safety Data

• Hazardous Substances Data: 704913-84-8(Hazardous Substances Data)

Usage

Uses

Used in Flavor and Fragrance Industry:
2-Furancarboxylic acid, 3-ethyl-, methyl ester (9CI) is used as a flavoring agent for enhancing the taste and aroma of various food products. Its fruity scent also makes it a popular ingredient in the production of fragrances, adding a pleasant aroma to personal care and household products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Furancarboxylic acid, 3-ethyl-, methyl ester (9CI) serves as a precursor for the synthesis of various compounds. Its unique chemical structure allows it to be a valuable building block in the development of new drugs and medicinal products.
Used in Agrochemical Industry:
2-Furancarboxylic acid, 3-ethyl-, methyl ester (9CI) is also utilized in the agrochemical industry as a starting material for the synthesis of different agrochemical compounds. Its role in this industry is crucial for the development of effective pesticides, herbicides, and other agricultural products.
Safety Precautions:
It is important to handle 2-Furancarboxylic acid, 3-ethyl-, methyl ester (9CI) with care, as it may be harmful if ingested, inhaled, or comes into contact with skin and eyes. To prevent any potential hazards, it should be stored in a cool, dry place away from incompatible substances.

Upstream product

• 31199-03-8 1,1-dimethoxypentan-3-one 
• 96-34-4 methyl chloroacetate 
• 934340-06-4 C₁₀H₁₈O₅ 

Downstream Products

• 934340-47-3 C₁₄H₁₃ClO₃ 
• 934340-48-4 C₁₄H₁₂Cl₂O₃ 
• 934340-49-5 C₁₅H₁₅ClO₄ 
• 704913-86-0 tert-butyl (3-ethyl-furan-2-yl)carbamate 

Relevant articles and documents

3-Substituted-(5-arylfuran-2-ylcarbonyl)guanidines as NHE-1 inhibitors

The C-3 substituents effect on NHE-1 inhibitory activity of (5-arylfuran-2-ylcarbonyl)guanidines, previously identified as potent NHE-1 inhibitors, was investigated. The introduction of amine or alkyl groups at the 3-position of the furan ring, next to the acylguanidine moiety, remarkably improves NHE-1 inhibitory potency. Especially the important finding is that 5-(2,5-dichloro)phenyl and 5-(2-methoxy-5-chloro)phenyl derivatives exhibit high NHE-1 inhibitory activities (IC50 0.02 μM) that match those of 3-unsubstituted derivatives.

Rhodium(I)-catalyzed nucleophilic ring-opening reactions of oxabicyclo adducts derived from the [4 + 2]-cycloaddition of 2-imido-substituted furans

A series of 2-imido-substituted furans containing tethered unsaturation were prepared by the addition of the lithium carbamate of furan-2-ylcarbamic acid tert-butyl ester to a solution of the mixed anhydride of an appropriately substituted 3-butenoic acid

A new strategy toward indole alkaloids involving an intramolecular cycloaddition/rearrangement cascade

The intramolecular Diels-Alder reaction between an amidofuran moiety tethered onto an indole component was examined as a strategy for the synthesis of Aspidosperma alkaloids. Furanyl carbamate 23 was acylated using the mixed anhydride 26 to provide amidof