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Butanedioic acid, [(2,4-dinitrophenyl)hydrazono]-, dimethyl ester is a chemical compound with the molecular formula C10H10N4O8. It is a derivative of butanedioic acid, also known as succinic acid, which has been modified by the addition of a (2,4-dinitrophenyl)hydrazono group and two methyl ester groups. Butanedioic acid, [(2,4-dinitrophenyl)hydrazono]-, dimethyl ester is characterized by its yellow crystalline appearance and is soluble in organic solvents such as ethanol and acetone. It is primarily used in chemical research and analysis, particularly in the study of metal chelation and as a reagent in various analytical techniques. Due to its complex structure and potential reactivity, it is important to handle Butanedioic acid, [(2,4-dinitrophenyl)hydrazono]-, dimethyl ester with care, following proper safety protocols.

6745-50-2

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6745-50-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6745-50-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,4 and 5 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6745-50:
(6*6)+(5*7)+(4*4)+(3*5)+(2*5)+(1*0)=112
112 % 10 = 2
So 6745-50-2 is a valid CAS Registry Number.

6745-50-2Downstream Products

6745-50-2Relevant academic research and scientific papers

Synthesis, Structure, and Biological Activity of (2Z)-2-[(2,4-Dinitrophenyl)hydrazinylidene]butanedioic Acid Esters

Mukovoz,Dankovtseva,Mukovoz,Slepukhin,Ganebnykh,Sizentsov,Danilova

, p. 1 - 7 (2019/04/13)

Dialkyl (2Z)-2-[(2,4-dinitrophenyl)hydrazinylidene]butanedioates have been synthesized by reaction of dialkyl (2Z)-2-hydroxybut-2-enedioates with 2,4-dinitrophenylhydrazine, and their structure has been studied by IR and 1H NMR spectroscopy, ma

Reactions of Tertiary Allylamines with Dimethyl Acetylenedicarboxylate

Kandeel, Kamal A.,Vernon, John M.

, p. 2023 - 2026 (2007/10/02)

The reaction of some tertiary allylamines with dimethyl acetylenedicarboxylate in acetonitrile results in the formation of 1:1 adducts via rearrangement of the allyl group from nitrogen to carbon.

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