6943-09-5 Usage
Molecular structure
2,2-dimethyl-5-(2,4,6-trimethylbenzylidene)-1,3-dioxane-4,6-dione has a complex molecular structure consisting of a dioxane ring with various substituents such as methyl and trimethylbenzyl groups.
Type of compound
It is an organic compound, which means it is primarily composed of carbon, hydrogen, and other elements found in living organisms.
Uses
This chemical is commonly used as a dye intermediate and in the production of colorants and pigments, making it suitable for various applications such as inks, plastics, and textiles.
Coloration properties
2,2-dimethyl-5-(2,4,6-trimethylbenzylidene)-1,3-dioxane-4,6-dione is known for its strong coloration properties, which contribute to its widespread use in industries that require vibrant colors.
Hazardous nature
It is important to handle this chemical with caution as it may be hazardous to human health and the environment if not properly managed. This means that proper safety measures and disposal methods should be followed to minimize potential risks.
Versatility
The compound's unique properties and wide range of industrial uses make it a versatile option for various applications, from coloration to the production of different materials.
Check Digit Verification of cas no
The CAS Registry Mumber 6943-09-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,4 and 3 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6943-09:
(6*6)+(5*9)+(4*4)+(3*3)+(2*0)+(1*9)=115
115 % 10 = 5
So 6943-09-5 is a valid CAS Registry Number.
6943-09-5Relevant articles and documents
Towards organo-click reactions: Development of pharmaceutical ingredients by using direct organocatalytic bio-mimetic reductions
Ramachary, Dhevalapally B.,Reddy, G. Babul
, p. 4463 - 4468 (2008/09/19)
Economic and environmentally friendly bio-mimetic one-pot three and four-component Knoevenagel-hydrogenation (K-H), five-component Knoevenagel-hydrogenation-alkylation (K-H-A) and six-component Knoevenagel-hydrogenation-alkylation-Huisgen cycloaddition (K-H-A-HC) reactions of aldehydes, CH-acids, o-phenylenediamine, alkyl halides and azides using proline, proline-metal carbonate and proline-metal carbonate-Cu I-catalysis, respectively have been developed. Many of K-H and K-H-A compounds have direct application in pharmaceutical chemistry. The Royal Society of Chemistry.
