5744-65-0 Usage
Uses
Used in Solvent Applications:
1,1,3,3-Tetramethoxybutane is used as a solvent due to its ability to dissolve a wide range of substances, making it valuable in various chemical processes and industries.
Used in Fragrance Production:
In the fragrance industry, 1,1,3,3-Tetramethoxybutane is used as a component in the creation of various scented products, capitalizing on its fruity odor to enhance the olfactory profiles of these products.
Used in Pharmaceutical Synthesis:
1,1,3,3-Tetramethoxybutane is utilized as an intermediate chemical in the synthesis of pharmaceuticals, contributing to the development of new medications and therapeutic agents.
Used in Organic Compound Synthesis:
1,1,3,3-Tetramethoxybutane also serves as an intermediate in the synthesis of other organic compounds, highlighting its importance in the broader field of organic chemistry and chemical engineering.
It is crucial to handle 1,1,3,3-Tetramethoxybutane with care and adhere to proper safety measures in both laboratory and industrial settings to ensure the safety of individuals and the integrity of the processes in which it is involved.
Check Digit Verification of cas no
The CAS Registry Mumber 5744-65-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,4 and 4 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5744-65:
(6*5)+(5*7)+(4*4)+(3*4)+(2*6)+(1*5)=110
110 % 10 = 0
So 5744-65-0 is a valid CAS Registry Number.
5744-65-0Relevant academic research and scientific papers
DAST promotes the synthesis of new 5-(trifluoromethyl)-3-(1,1-difluoroethan-2-yl)-1H-pyrazoles
Bonacorso, Helio G.,Porte, Liliane M.F.,Cechinel, Cleber A.,Paim, Gisele R.,Deon, Everton D.,Zanatta, Nilo,Martins, Marcos A.P.
scheme or table, p. 1392 - 1394 (2009/06/08)
This study describes, firstly, the synthesis of a new precursor, 4,6,6-trimethoxy-1,1,1-trifluorohex-3-en-2-one (1), from the trifluoroacetylation reaction of 1,1,3,3-tetramethoxybutane, in 65% yields. Afterwards, the reaction of 1 with two hydrazines (NH
