66104-54-9 Usage
Chemical structure
Aromatic ether with three propoxy groups attached to a benzene ring
Aromatic ether
Contains an ether functional group (R-O-R') within an aromatic system
Propoxy groups
Three propoxy (-OCH2CH2CH3) groups attached to the benzene ring
Industrial applications
Used as a solvent and a precursor in the synthesis of other organic compounds
Production
Useful for the production of polymers and resins
Fields of application
Organic chemistry and material science
Hazardous properties
Potential hazards require careful handling and safety precautions
Physical state
Likely a liquid at room temperature, based on molecular size and structure
Solubility
Soluble in organic solvents, such as alcohols, ethers, and hydrocarbons
Reactivity
May react with strong acids, strong bases, and oxidizing agents
Stability
Stable under normal temperature and pressure conditions, but sensitive to heat, light, and moisture
Toxicity
Potentially toxic, depending on exposure levels and duration
Environmental impact
May have negative environmental effects if not properly disposed of or released into the environment
Storage
Should be stored in a cool, dry, and well-ventilated area, away from heat, sparks, and open flames
Check Digit Verification of cas no
The CAS Registry Mumber 66104-54-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,1,0 and 4 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 66104-54:
(7*6)+(6*6)+(5*1)+(4*0)+(3*4)+(2*5)+(1*4)=109
109 % 10 = 9
So 66104-54-9 is a valid CAS Registry Number.
InChI:InChI=1/C15H24O3/c1-4-7-16-13-10-14(17-8-5-2)12-15(11-13)18-9-6-3/h10-12H,4-9H2,1-3H3
66104-54-9Relevant academic research and scientific papers
Wang, Denan,Mirzaei, Saber,Lindeman, Sergey V.,Rathore, Rajendra
, (2019)
Synthesizing novel electron-rich calix[n]arene derivatives to alter the electronic properties of calixarene-based materials has been one of the long-standing interests. Herein, two new electron-rich calix[n]arenes (n = 4 and 8) with different sizes were s
SYNTHESIS OF PHLOROGLUCINOL TRIALKYL ETHERS
Kirillova, K. M.,Skvortsova, T. A.,Nikonova, L. Z.,Chugunov, Yu. V.,Igonin, V. B.,Mukhtarov, A. Sh.
, p. 427 - 430 (2007/10/02)
The alkylation of phloroglucinol dialkyl ethers with alcohols or alkyl halides leads, depending on the reaction conditions, either to products of O- or C- alkylation, or to C,O-alkylation products.Reaction conditions were found which enable us to obtain pure phloroglucinol trialkyl ethers.A convenient preparative method for the synthesis of phloroglucinol trialkyl ethers consists in the alkylation of phloroglucinol dialkyl ethers in a two-phase system in presence of phase-transfer catalysts.
