1906-57-6 Usage
Description
Potassium ethyl oxalate is an organic compound with the chemical formula C4H5KO4. It is a white crystalline solid that is soluble in water and is commonly used as a reagent in various chemical reactions.
Uses
Used in Chemical Synthesis:
Potassium ethyl oxalate is used as a reagent for the preparation of oxalic acid ethyl ester 2-oxo-3-phenyl-propyl ester by reacting with 1-bromo-3-phenyl-acetone. This reaction is important in the synthesis of various organic compounds and pharmaceuticals.
In the Chemical Industry:
Potassium ethyl oxalate is used as a starting material for the synthesis of various organic compounds, including pharmaceuticals, dyes, and other specialty chemicals. Its versatility as a reagent makes it a valuable component in the chemical industry.
In the Pharmaceutical Industry:
As a reagent, potassium ethyl oxalate plays a role in the synthesis of pharmaceutical compounds. Its ability to react with various starting materials allows for the creation of a wide range of drug candidates, contributing to the development of new medications.
In the Research and Development Sector:
Potassium ethyl oxalate is also utilized in research and development laboratories for the synthesis of novel compounds and the exploration of new chemical reactions. Its use in this sector helps to advance scientific knowledge and drive innovation in the field of chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 1906-57-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,0 and 6 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1906-57:
(6*1)+(5*9)+(4*0)+(3*6)+(2*5)+(1*7)=86
86 % 10 = 6
So 1906-57-6 is a valid CAS Registry Number.
InChI:InChI=1/C4H6O4.K/c1-2-8-4(7)3(5)6;/h2H2,1H3,(H,5,6);/q;+1/p-1
1906-57-6Relevant articles and documents
A DEVELOPING AGENT PRECURSOR FOR LASER MARKABLE COMPOSITIONS
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Paragraph 0139, (2019/01/07)
The invention relates to novel laser markable compositions comprising developing agent precursors according to formula (I).
Ligand free palladium catalyzed decarboxylative cross-coupling of aryl halides with oxalate monoester salts
Li, Yan,Chen, Huan-Huan,Wang, Chu-Fei,Xu, Xiao-Lan,Feng, Yi-Si
, p. 5796 - 5799 (2012/10/29)
Ligand free Pd-catalyzed decarboxylative cross-coupling of potassium oxalate monoester and derivatives with aryl iodides and bromides is described. Functionalized aromatic esters can be efficiently synthesized via this method with only 1.0 mol % Pd(OAc)2 catalyst without any phosphine ligand. This method illustrates an inexpensive and operationally simple method for the preparation of aromatic esters and acids, which is especially beneficial for a large scale synthesis.
Synthesis of aromatic esters via Pd-catalyzed decarboxylative coupling of potassium oxalate monoesters with aryl bromides and chlorides
Shang, Rui,Fu, Yao,Li, Jia-Bin,Zhang, Song-Lin,Guo, Qing-Xiang,Liu, Lei
supporting information; experimental part, p. 5738 - 5739 (2009/09/25)
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