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2,3,4-Furantricarboxylic acid triethyl ester is a chemical compound with the molecular formula C13H14O5. It is a triester of furan-2,3,4-tricarboxylic acid and ethyl alcohol, characterized by its colorless liquid form, fruity odor, and solubility in organic solvents. 2,3,4-Furantricarboxylic acid triethyl ester is insoluble in water and is commonly used as a precursor for the synthesis of various organic compounds, as well as a solvent or intermediate in chemical reactions.

7251-41-4

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7251-41-4 Usage

Uses

Used in Organic Synthesis:
2,3,4-Furantricarboxylic acid triethyl ester is used as a precursor for the synthesis of various organic compounds, contributing to the development of new chemical entities and materials.
Used in Chemical Reactions:
2,3,4-Furantricarboxylic acid triethyl ester is used as a solvent or intermediate in chemical reactions, facilitating the progress of various processes and reactions in the laboratory and industrial settings.
Used in Industrial Applications:
2,3,4-Furantricarboxylic acid triethyl ester is used in various industrial applications, leveraging its chemical structure and properties to enhance the performance of different products and processes.

Check Digit Verification of cas no

The CAS Registry Mumber 7251-41-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,5 and 1 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7251-41:
(6*7)+(5*2)+(4*5)+(3*1)+(2*4)+(1*1)=84
84 % 10 = 4
So 7251-41-4 is a valid CAS Registry Number.
InChI:InChI=1/C13H16O7/c1-4-17-11(14)8-7-20-10(13(16)19-6-3)9(8)12(15)18-5-2/h7H,4-6H2,1-3H3

7251-41-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name triethyl furan-2,3,4-tricarboxylate

1.2 Other means of identification

Product number -
Other names furan-2,3,4-tricarboxylic acid triethyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7251-41-4 SDS

7251-41-4Downstream Products

7251-41-4Relevant academic research and scientific papers

Synthesis of furan-2,3,4-tricarboxylate in biphasic water-Et2O solvent system

Sabbaghan, Maryam,Yousefi, Ali

, p. 804 - 807 (2015)

[Figure not available: see fulltext.] The reaction of dialkyl acetylenedicarboxylates with ethyl bromopyruvate or α-chlorocarbonyl compounds in the presence of 1,4-diazabicyclo[ 2.2.2]octane led to furan-2,3,4-tricarboxylates or the related 2-acetylfuran-3,4-dicarboxylates in excellent yield.

Efficient synthesis of 2,3,4-trisubstituted furans from the reaction of activated acetylenes with ethyl bromopyruvate in the presence of enaminones

Yavari, Issa,Hossaini, Zinatossadat,Sabbaghan, Maryam

experimental part, p. 945 - 948 (2009/09/28)

The reaction of dialkyl acetylenedicarboxylates or diaroylacetylenes with ethyl bromopyruvate in the presence of enaminones led to 2-ethyl 3,4-dialkyl 4-bromo-4,5-dihydro-2,3,4-furantricarboxylates or ethyl 3,4-diaroyl-4-bromo-4,5- dihydro-2-furancarboxyl

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