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2,2-dimethyl-1,3-dioxane-4,5,6-trione 5-(phenylhydrazone) is a hydrazone derivative with a complex chemical structure, characterized by a nitrogen atom double-bonded to a carbon atom attached to a phenyl group. This solid compound at room temperature is primarily utilized in chemical research and synthesis as a reagent or intermediate. Its potential applications in pharmaceutical and medicinal chemistry are under investigation, with further research required to elucidate its full properties and uses.

75307-67-4

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75307-67-4 Usage

Uses

Used in Chemical Research and Synthesis:
2,2-dimethyl-1,3-dioxane-4,5,6-trione 5-(phenylhydrazone) is used as a reagent or intermediate in chemical research and synthesis processes for its unique structural properties and potential to facilitate the creation of new compounds.
Used in Pharmaceutical and Medicinal Chemistry:
Although further research is needed, 2,2-dimethyl-1,3-dioxane-4,5,6-trione 5-(phenylhydrazone) may be used as a potential candidate in pharmaceutical and medicinal chemistry due to its distinctive hydrazone functional group, which could offer novel therapeutic or diagnostic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 75307-67-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,3,0 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 75307-67:
(7*7)+(6*5)+(5*3)+(4*0)+(3*7)+(2*6)+(1*7)=134
134 % 10 = 4
So 75307-67-4 is a valid CAS Registry Number.

75307-67-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-dimethyl-5-(phenylhydrazinylidene)-1,3-dioxane-4,6-dione

1.2 Other means of identification

Product number -
Other names -

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 -
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More Details:75307-67-4 SDS

75307-67-4Relevant academic research and scientific papers

Rapid and clean synthesis of 5-arylhydrazones of Meldrum's acid using polymer supported Meldrum's acid anion

Bandgar,Tavhare,Pandit

, p. 721 - 723 (2007/10/03)

Polymer supported Meldrum's acid anion is treated with various aryl diazonium fluoroborates at 25°C in acetonitrile to give corresponding 5- arylhydrazones of Meldrum's acid in good yield. Isolation of pure products by simple filtration and evaporation is

Reactive Nitrogenous Molecules from Meldrum's Acid Derivatives, Pyrrole-2,3-diones, and Isoxazolones

Briehl, Horst,Lukosch, Adelheid,Wentrup, Curt

, p. 2772 - 2779 (2007/10/02)

Flash vacuum pyrolysis of 5-(aminomethylidene)-2,2-dimethyl-1,3-dioxane-4,6-diones (Meldrum's acid derivatives) 12 gives 4-hydroxyquinolines/4-quinolones 15 or 3-enaminoacroleins 22 in good to excellent yields.Intermediate (aminomethylene)ketenes and imidoylketenes are directly observed and their transformation into product 22 monitored by low-temperature IR spectroscopy.Imidoylketenes are also formed and observed upon thermal CO extrusion from pyrrole-2,3-diones 16.Isocyanoamines and fulminates are generated by pyrolysis of hydrazono- or oximino-Meldrum's acid derivatives 32 and 39, monitored by IR spectroscopy, and found to rearrange to cyanamides and cyanates, depending on substituents.The thermal reactions of isoxazol-5(4H)-ones and Meldrum's acid derivatives are compared and discussed.

Introduction of Oxygen Functions into the α-Position of β-Diketones, 4: "Hydroxy- and Oxo-Meldrum's Acids"

Bouillon, Guenther,Schank, Kurt

, p. 2630 - 2635 (2007/10/02)

Synthesis and properties of 5-hydroxy-, 5-acyloxy-, 5-oxo- and 5,5-dihydroxy-2,2-dialkyl-1,3-dioxane-4,6-diones (6, 5/9, 7, 10) are described.

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