14064-21-2 Usage
Description
2-FURALDEHYDE DIMETHYLHYDRAZONE, also known as 2-furaldehyde N,N-dimethylhydrazone, is an organic compound that has been studied through combined matrix isolation FTIR and theoretical DFT(B3LYP)/6-311++G(d,p) methods. It is characterized by its ability to react with various chemical compounds, making it a versatile molecule in the field of organic chemistry.
Uses
Used in Chemical Synthesis:
2-FURALDEHYDE DIMETHYLHYDRAZONE is used as a synthetic intermediate for the preparation of various chemical compounds, such as furyl-1,4-quinone and hydroquinones. It is particularly useful in the reaction with benzoand naphthoquinones to produce dimethylaminohydrazonofurylquinones.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-FURALDEHYDE DIMETHYLHYDRAZONE is used as a key component in the synthesis of certain drugs, taking advantage of its reactivity with other molecules to create new therapeutic agents.
Used in Research and Development:
2-FURALDEHYDE DIMETHYLHYDRAZONE is also utilized in research and development settings, where its chemical properties are explored for potential applications in the creation of new materials, catalysts, or other advanced chemical products.
Used in Analytical Chemistry:
In analytical chemistry, 2-FURALDEHYDE DIMETHYLHYDRAZONE can be employed as a reagent for the detection and identification of specific compounds, leveraging its unique chemical interactions to provide insights into the structure and composition of various substances.
Check Digit Verification of cas no
The CAS Registry Mumber 14064-21-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,0,6 and 4 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 14064-21:
(7*1)+(6*4)+(5*0)+(4*6)+(3*4)+(2*2)+(1*1)=72
72 % 10 = 2
So 14064-21-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H10N2O/c1-9(2)8-6-7-4-3-5-10-7/h3-6H,1-2H3/b8-6+
14064-21-2Relevant articles and documents
Polyoxometalate-Driven Ease Conversion of Valuable Furfural to trans- N, N-4,5-Diaminocyclopenten-2-ones
Tzani, Marina A.,Fountoulaki, Stella,Lykakis, Ioannis N.
, p. 2601 - 2615 (2022/02/10)
We investigated the catalytic efficacy of silicotungstic acid (H4SiW12O40) polyoxometalate (POM) toward the reaction between furfural and amines that selectively yields trans-N,N-4,5-substituted-diaminocyclopenten-2-ones (trans-DACPs). H4SiW12O40 facilita
THERAPEUTIC CURE-PRO COMPOUNDS FOR TARGETED DEGRADATION OF BET DOMAIN PROTEINS, AND METHODS OF MAKING AND USING THEM
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Paragraph 0325-0327, (2022/02/15)
The present application is directed to a therapeutically useful compound, comprised of two monomers that are linked to each other through two or more reversible covalent bonds. Each monomer is a polyfunctionalized molecule comprising a bioorthogonal linker element and ligand or pharmacophore, wherein the linker and ligand/pharmacophore are covalently coupled to each other either directly or through an optional connector moiety.
Chemical cascades in water for the synthesis of functionalized aromatics from furfurals
Higson, Sally,Subrizi, Fabiana,Sheppard, Tom D.,Hailes, Helen C.
supporting information, p. 1855 - 1858 (2016/04/19)
One-pot synthetic routes from furfurals to polysubstituted aromatic compounds have been developed in water, without the need for any organic solvents. The reaction proceeds via an uncatalysed, one-pot reaction cascade through formation of a hydrazone derivative, in situ cycloaddition with a dienophile, then aromatisation. A range of substituted phthalimides can be accessed with complete control over the substitution pattern. The reaction was also extended to other dienophiles and the diene 2-furylacrolein. The phthalimide products were further elaborated to produce a variety of polysubstituted benzenes including pharmaceutically relevant compounds.
