127457-63-0 Usage
Uses
Used in Pharmaceutical Industry:
3-[2-(2-benzyloxyethoxy)ethoxy]propanoic acid is used as a pharmaceutical intermediate for the synthesis of various drugs. Its complex structure and aromatic properties make it a valuable component in the development of new medicinal compounds with potential therapeutic applications.
Used in Cosmetics Industry:
In the cosmetics industry, 3-[2-(2-benzyloxyethoxy)ethoxy]propanoic acid is used as an active ingredient for its potential skin conditioning and moisturizing properties. Its ability to interact with the skin's natural moisture barrier may contribute to improved skin hydration and overall skin health.
Used in Agrochemical Industry:
3-[2-(2-benzyloxyethoxy)ethoxy]propanoic acid is utilized as a precursor in the synthesis of agrochemicals, such as pesticides and herbicides. Its complex structure and reactivity may offer new avenues for the development of more effective and environmentally friendly agricultural products.
Used in Material Science:
In the field of material science, 3-[2-(2-benzyloxyethoxy)ethoxy]propanoic acid is employed as a component in the development of advanced materials with specific properties. Its potential use in polymer synthesis or as a modifier for existing materials could lead to the creation of new materials with improved characteristics for various applications.
Used in Research and Development:
3-[2-(2-benzyloxyethoxy)ethoxy]propanoic acid serves as a valuable research compound for scientists and researchers. Its unique structure and properties provide a foundation for exploring new chemical reactions, synthesis pathways, and potential applications in various fields, driving innovation and discovery.
Overall, the diverse applications of 3-[2-(2-benzyloxyethoxy)ethoxy]propanoic acid highlight its potential as a versatile compound with significant implications in multiple industries. Further research and development are necessary to fully understand its properties and harness its potential for practical use.
Check Digit Verification of cas no
The CAS Registry Mumber 127457-63-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,4,5 and 7 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 127457-63:
(8*1)+(7*2)+(6*7)+(5*4)+(4*5)+(3*7)+(2*6)+(1*3)=140
140 % 10 = 0
So 127457-63-0 is a valid CAS Registry Number.
127457-63-0Relevant academic research and scientific papers
Novel 3-O-pegylated carboxylate and 3-O-pegylated carbamate prodrugs of naltrexone for microneedle-enhanced transdermal delivery
Yerramreddy, Thirupathi Reddy,Milewski, Mikolaj,Penthala, Narsimha Reddy,Stinchcomb, Audra L.,Crooks, Peter A.
scheme or table, p. 3280 - 3283 (2010/08/19)
A small library of novel 3-O-pegylated carboxylate prodrugs (4a-4b) and 3-O-pegylated carbamate prodrugs (9a-9b) of naltrexone were synthesized. The goal behind the design of these prodrugs was to investigate their potential for microneedle-enhanced transdermal delivery. All the synthesized 3-O-pegylated carboxylate prodrugs (4a-4b) and 3-O-pegylated carbamate prodrugs (9a-9b) of naltrexone were found to have adequate stability in a transdermal formulation and improved apparent solubility compared to naltrexone. Viscosity effects were postulated to be responsible for the observed non-linearity in the flux-concentration profile of these prodrugs.
ω-HYDROXY AMD ω-AMINO-CARBOXYLIC ACID DERIVATIVES FOR THE PREPARATION OF ESTERS AND AMIDE CROWN ETHERS
Houghton, Roy P.,Southby, David T.
, p. 3199 - 3210 (2007/10/02)
An oxymercuration reaction bentween methyl acrylate and the monobenzyl ethers (3) of mono-, di-, and triethylene glycol, followed by reduction with sodium borohydride, gives the expected polyether esters (4).These are converted by standard procedures into
