84877-70-3 Usage
Uses
Used in Pharmaceutical Industry:
[2-(benzyloxy)ethoxy]benzene is used as a solvent and intermediate for the synthesis of various pharmaceutical compounds. Its application in this industry is due to its ability to facilitate the production of essential drugs and contribute to the development of novel therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical industry, [2-(benzyloxy)ethoxy]benzene is utilized as a solvent and intermediate in the synthesis of agrochemicals. Its use is attributed to its capacity to aid in the production of chemicals that are vital for agricultural purposes, such as pesticides and fertilizers.
Used in Polymer Production:
[2-(benzyloxy)ethoxy]benzene is employed in the production of polymers, where it serves as a chemical building block. Its application in this field is due to its ability to contribute to the development of new polymer materials with specific properties and potential applications in various industries.
Used in Organic Reactions:
BEEB is used as a chemical building block for various organic reactions, allowing for the synthesis of a wide range of organic compounds. Its application in this area is due to its versatility and the potential for creating diverse chemical products through its use in different reaction pathways.
Check Digit Verification of cas no
The CAS Registry Mumber 84877-70-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,8,7 and 7 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 84877-70:
(7*8)+(6*4)+(5*8)+(4*7)+(3*7)+(2*7)+(1*0)=183
183 % 10 = 3
So 84877-70-3 is a valid CAS Registry Number.
84877-70-3Relevant articles and documents
Vanadium-Catalyzed Oxidative Debenzylation of O-Benzyl Ethers at ppm Level
Urgoitia, Garazi,SanMartin, Raul,Herrero, María Teresa,Domínguez, Esther
supporting information, p. 3307 - 3312 (2016/10/21)
An advantageous methodology for the oxidative debenzylation of ethers has been developed. Very low amounts of a catalyst system based on vanadyl acetylacetonate and a triazole type pincer ligand allow the selective oxidative cleavage of a number of O-benzyl ethers in the presence of oxygen as the sole oxidant. The methodology tolerates a number of functional groups such as halo-, alkoxy-, or trifluoromethylarenes, alkyne, alkene, ether, and acetal units. Large-scale deprotections can be also carried out by the optimized procedure, which is amenable to enantioenriched reactants as well. (Figure presented.).
