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25007-54-9

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25007-54-9 Usage

General Description

Dimethyl 2-oxobutanedioate is a chemical compound with the molecular formula C6H8O5. It is also known as dimethyl pyruvate, and it is an ester of pyruvic acid. dimethyl 2-oxobutanedioate is often used as a reagent in organic synthesis, specifically in the formation of various pharmaceuticals and other organic compounds. Dimethyl 2-oxobutanedioate is a colorless, pleasant-smelling liquid with a melting point of -57°C and a boiling point of 119-120°C. It is soluble in water and ethanol, and it is commonly used as a precursor in the synthesis of pyruvate-derived compounds. Additionally, it is known to have antimicrobial and antioxidant properties, making it potentially useful in various industrial and medicinal applications.

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

25007-54-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl 2-oxobutanedioate

1.2 Other means of identification

Product number -
Other names Dimethyl 2-oxosuccinate

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:25007-54-9 SDS

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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