1687-61-2 Usage
Uses
Used in Flavor and Fragrance Industry:
6-Ethyl-m-cresol is used as a flavoring agent and fragrance for its characteristic odor, enhancing the sensory experience of perfumes and soaps.
Used in Pharmaceutical and Cosmetic Industries:
6-Ethyl-m-cresol is used as a preservative in the pharmaceutical and cosmetic industries, leveraging its antimicrobial properties to prevent the growth of microorganisms and extend the shelf life of products.
Used in Chemical Intermediates:
6-Ethyl-m-cresol is used as a chemical intermediate in the production of various chemicals, contributing to the synthesis of a wide range of compounds.
Used in Polymer Production:
6-Ethyl-m-cresol is used as a stabilizer in the production of polymers, improving the stability and performance of the final polymer products.
Check Digit Verification of cas no
The CAS Registry Mumber 1687-61-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,8 and 7 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1687-61:
(6*1)+(5*6)+(4*8)+(3*7)+(2*6)+(1*1)=102
102 % 10 = 2
So 1687-61-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H12O/c1-3-8-5-4-7(2)6-9(8)10/h4-6,10H,3H2,1-2H3
1687-61-2Relevant academic research and scientific papers
Halide-free ethylation of phenol by multifunctional catalysis using phosphinite ligands
Carrion, M. Carmen,Cole-Hamilton, David J.
, p. 4527 - 4529 (2008/09/18)
The ortho-alkylation of phenols or aniline by catalytic C-H activation and multifunctional catalysis is described. The Royal Society of Chemistry 2006.
Catalytic ethylation of phenols
Agaev,Shakhtakhtinskaya,Eminov,Guliev
, p. 651 - 653 (2007/10/03)
Alkylation of phenol and cresols with ethanol in the presence of iron-aluminum catalyst was studied.
Thermolysis of alkylated 2-cyclohexenones and related monoterpenoid ketones
Lange, Gordon L.,Pereira, Vincent A.,Weedle, Michael
, p. 1639 - 1644 (2007/10/02)
2-Cyclohexenone and three methylated cyclohexenones were thermolyzed at 400 deg C for 20 hours to give conversions to products in the range 11 to 45 percent.When three monoterpenes containing the cyclohexenone moiety were thermolyzed under the same conditions the conversions were over 75 percent.The major products formed were alkylated benzenes, alkylated phenols, and double bond isomers of the starting enones.Mechanisms are proposed to account for these products.
