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Methyl 5-(acetoxymethyl)furan-2-carboxylate is a chemical compound with the molecular formula C8H8O5. It is a derivative of furan, a heterocyclic organic compound consisting of a five-membered ring with four carbon atoms and one oxygen atom. In this specific compound, the 5-position of the furan ring is substituted with an acetoxymethyl group, which is an acetate ester of a methyl group. The 2-position of the furan ring is substituted with a carboxylate group, which is a negatively charged carboxylic acid group. Methyl 5-(acetoxyMethyl)furan-2-carboxylate is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, and it is known for its versatile reactivity and potential applications in organic chemistry.

2144-38-9

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2144-38-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2144-38-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,4 and 4 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2144-38:
(6*2)+(5*1)+(4*4)+(3*4)+(2*3)+(1*8)=59
59 % 10 = 9
So 2144-38-9 is a valid CAS Registry Number.

2144-38-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 5-(acetoxymethyl)furan-2-carboxylate

1.2 Other means of identification

Product number -
Other names 5-acetoxymethyl-2-carbomethoxyfuran

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 -
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More Details:2144-38-9 SDS

2144-38-9Relevant academic research and scientific papers

2-(guanidiniocarbonyl)furans as a new class of potential anion hosts: Synthesis and first binding studies

Schmuck, Carsten,Machon, Uwe

, p. 4385 - 4392 (2007/10/03)

The synthesis of a new class of potential anion hosts, the 2-(guanidiniocarbonyl)furans 5a-d, is presented in this study. The facile decomposition of furans under acidic conditions makes the synthesis of these compounds challenging. First binding studies showed that the (guanidiniocarbonyl)furans are much more acidic (pKa ≈5.5) than the analogous pyrroles (pKa ≈ 7) previously introduced by us for oxoanion binding in aqueous solvents. Hence, anion binding with the furan derivatives occurs only in acidic solutions below pH = 5. Therefore, carboxylates are not bound efficiently, whereas, for example, the less basic hydrogen sulfate is bound by 5b with an association constant of K = 600 M -1 in aqueous DMSO even in the presence of a large excess of buffer. Wiley-VCH Verlag GmbH & Co. KGaA, 2006.

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