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Oxalic acid 1-ethyl ester, also known as ethyl oxalacetate, is an organic compound derived from oxalic acid. It is a colorless liquid with a distinctive odor and is used as a synthetic intermediate in various chemical reactions. Its chemical structure allows for the formation of various compounds with different applications across different industries.

617-37-8

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617-37-8 Usage

Uses

Used in Pharmaceutical Industry:
Oxalic acid 1-ethyl ester is used as a synthetic intermediate for the production of 2-substituted 3-aryl-4(3H)-quinazolinones, which possess anticonvulsant activities. These compounds are valuable in the development of medications to treat seizures and other related neurological disorders.
Used in Biochemical Research:
In the field of biochemical research, oxalic acid 1-ethyl ester is utilized to prepare nonbenzamidine tetrazole derivatives. These derivatives serve as factor Xa inhibitors, which are essential in the study and treatment of blood clotting disorders and related conditions.
Used in Chemical Synthesis:
Oxalic acid 1-ethyl ester is also employed as a synthetic intermediate in the chemical synthesis of various compounds, contributing to the development of new materials and products in the chemical industry. Its versatility in chemical reactions makes it a valuable component in the synthesis of a wide range of substances with diverse applications.

Check Digit Verification of cas no

The CAS Registry Mumber 617-37-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,1 and 7 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 617-37:
(5*6)+(4*1)+(3*7)+(2*3)+(1*7)=68
68 % 10 = 8
So 617-37-8 is a valid CAS Registry Number.
InChI:InChI=1/C4H6O4/c1-2-8-4(7)3(5)6/h2H2,1H3,(H,5,6)

617-37-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Ethoxy-2-oxoacetic acid

1.2 Other means of identification

Product number -
Other names 2-ethoxy-2-oxoacetic acid

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:617-37-8 SDS

617-37-8Relevant articles and documents

Metal-Free Oxidative C=C Bond Cleavage of Electron-Deficient Enamines Promoted by tert -Butyl Hydroperoxide

Adib, Mehdi,Pashazadeh, Rahim,Gohari, Seyed Jamal Adin,Shahsavari, Fatemeh

supporting information, p. 1481 - 1485 (2017/08/15)

A novel tert -butyl hydroperoxide (TBHP)-promoted oxidative C=C double-bond cleavage of enamines is described. Heating a solution of an electron-deficient enamine in chlorobenzene at 80 °C in the presence of TBHP for two hours led to cleavage of the C=C bond. This study offers a new strategy to carry out C=O double-bond formation by the use of TBHP.

Template-free sol–gel synthesis of high surface area mesoporous silica based catalysts for esterification of di-carboxylic acids

More, Pavan M.,Umbarkar, Shubhangi B.,Dongare, Mohan K.

, p. 1247 - 1253 (2016/10/13)

High surface area mesoporous silica based catalysts have been prepared by a simple hydrolysis/sol–gel process without using any organic template and hydrothermal treatment. A controlled hydrolysis of ethyl silicate-40, an industrial bulk chemical, as a silica precursor, resulted in the formation of very high surface area (719?m2/g) mesoporous (pore size 67?? and pore volume 1.19?cc/g) silica. The formation of mesoporous silica has been correlated with the polymeric nature of the ethyl silicate-40 silica precursor which on hydrolysis and further condensation forms long chain silica species which hinders the formation of a close condensed structure thus creating larger pores resulting in the formation of high surface mesoporous silica. Ethyl silicate-40 was used further for preparing a solid acid catalyst by supporting molybdenum oxide nanoparticles on mesoporous silica by a simple hydrolysis sol–gel synthesis procedure. The catalysts showed very high acidity as determined by NH3-TPD with the presence of Lewis as well as Br?nsted acidity. These catalysts showed very high catalytic activity for esterification; a typical acid catalyzed organic transformation of various mono- and di-carboxylic acids with a range of alcohols. The in situ formed silicomolybdic acid heteropoly-anion species during the catalytic reactions were found to be catalytically active species for these reactions. Ethyl silicate-40, an industrial bulk silica precursor, has shown a good potential for its use as a silica precursor for the preparation of mesoporous silica based heterogeneous catalysts on a larger scale at a lower cost.

Oxidation of β-dicarbonyl compounds with tert-butyl hydroperoxide in the presence of vanadyl acetylacetonate

Stepovik,Gulenova,Kalacheva,Potkina, A. Yu.

experimental part, p. 550 - 558 (2011/06/23)

Oxidation of β-dicarbonyl compounds with tert-butyl hydroperoxide in the presence of vanadyl acetylacetonate (benzene, 20°C) involves the activated methylene group with intermediate formation of trioxo derivatives and is accompanied by decomposition of carbon skeleton. The oxidation products are carbon dioxide, carboxylic acids, and tert-butyl and peroxy esters derived from the latter.

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