14804-37-6 Usage
Uses
Used in Chemical Industry:
Benzene, methoxypentamethylis used as a solvent in various industrial processes due to its ability to dissolve a wide range of substances. Its solubility properties make it a valuable component in the production of dyes, paints, and adhesives.
Used in Pharmaceutical Industry:
As a key ingredient in the synthesis of pharmaceutical compounds, benzene, methoxypentamethylplays a crucial role in the development of new drugs and medications. Its unique chemical properties allow for the creation of novel therapeutic agents with potential applications in various medical fields.
Used in Research and Development:
Benzene, methoxypentamethylis utilized in research laboratories for the study of chemical reactions and the development of new chemical processes. Its versatility as a solvent and its unique chemical structure make it an essential tool for scientific exploration and innovation.
Check Digit Verification of cas no
The CAS Registry Mumber 14804-37-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,8,0 and 4 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 14804-37:
(7*1)+(6*4)+(5*8)+(4*0)+(3*4)+(2*3)+(1*7)=96
96 % 10 = 6
So 14804-37-6 is a valid CAS Registry Number.
14804-37-6Relevant academic research and scientific papers
Onodera, Kazuyuki,Sakuragi, Hirochika,Tokumaru, Katsumi
, p. 2831 - 2832 (1980)
Irradiation of the charge transfer complex of hexamethylbenzene with oxygen at 313 nm in a mixture of methanol and benzene afforded methoxymethyl-pentamethylbenzene and methoxypentamethylbenzene.
Methylation of phenol and its derivatives with dimethyl carbonate in the presence of Mn2(CO)10, W(CO)6, and Co2(CO)8
Khusnutdinov,Shchadneva,Mayakova, Yu. Yu.
, p. 330 - 334 (2015/05/04)
Aryl methyl ethers were synthesized by reactions of phenol, substituted phenols, and α- and β-naphthols with dimethyl carbonate in the presence of manganese, tungsten, and cobalt carbonyls. Optimal reactant and catalyst ratios and reaction conditions were found to ensure selective formation of aryl methyl ethers.
