25007-54-9 Usage
Description
Dimethyl 2-oxobutanedioate, also known as dimethyl pyruvate, is a chemical compound with the molecular formula C6H8O5. It is an ester of pyruvic acid and is often used as a reagent in organic synthesis. This colorless, pleasant-smelling liquid has a melting point of -57°C and a boiling point of 119-120°C. It is soluble in water and ethanol and is commonly used as a precursor in the synthesis of pyruvate-derived compounds. Dimethyl 2-oxobutanedioate also possesses antimicrobial and antioxidant properties, making it potentially useful in various industrial and medicinal applications.
Uses
Used in Pharmaceutical Industry:
Dimethyl 2-oxobutanedioate is used as a reagent in the synthesis of various pharmaceuticals for its ability to form pyruvate-derived compounds, which are essential in the development of new drugs.
Used in Organic Synthesis:
Dimethyl 2-oxobutanedioate is used as a reagent in organic synthesis for the formation of various organic compounds, contributing to the creation of a wide range of chemical products.
Used in Antimicrobial Applications:
Dimethyl 2-oxobutanedioate is used as an antimicrobial agent for its ability to inhibit the growth of certain microorganisms, making it potentially useful in sanitizing products and medical applications.
Used in Antioxidant Applications:
Dimethyl 2-oxobutanedioate is used as an antioxidant for its ability to neutralize harmful free radicals, which can be beneficial in various industrial and medicinal applications to prevent oxidative damage.
Check Digit Verification of cas no
The CAS Registry Mumber 25007-54-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,0,0 and 7 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 25007-54:
(7*2)+(6*5)+(5*0)+(4*0)+(3*7)+(2*5)+(1*4)=79
79 % 10 = 9
So 25007-54-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H8O5/c1-10-5(8)3-4(7)6(9)11-2/h3H2,1-2H3
25007-54-9Relevant articles and documents
Thermal rearrangements of tetrahydroimidazo[1,5-b]isoxazole-2,3-dicarboxylates. Synthesis of 3H-imidazol-1-ium ylides and their silver derivatives
Co?kun, Necdet,?etin, Meliha
experimental part, p. 2053 - 2060 (2010/04/26)
Isoxazolines 2 from the cycloaddition of imidazoline 3-oxides 1 with DMAD undergo rearrangement to 3,4-dihydro-2H-imidazol-1-ium-1-(1,2-bis-methoxycarbonyl-2-oxo-ethanides) 3, which spontaneously undergo elimination to give 3H-imidazol-1-ium-1-(1,2-bis-me
Synthesis of β-Dicarbonyl Compounds via the Conjugate Addition of Benzaldoximate Anion to α,β-Acetylenic Carbonyl Compounds
Gomez, Virginia,Perez-Medrano, Arturo,Muchowski, Joseph M.
, p. 1219 - 1221 (2007/10/02)
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