137794-34-4 Usage
Uses
Used in Plastics Industry:
Phenol, 2,6-bis[[2-[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]phenyl]methyl]-4-nitrois used as a monomer or intermediate in the production of various types of plastics. Its ethoxy groups contribute to the flexibility and durability of the plastic materials, making them suitable for a range of applications, from packaging to construction.
Used in Disinfectants:
Phenol,
2,6-bis[[2-[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]phenyl]methyl]-4-nitrois utilized in the formulation of disinfectants due to its antimicrobial properties. The phenol base and nitro group provide effective germicidal action, making it suitable for use in cleaning and sanitizing products, particularly in healthcare and food processing environments.
Used in Pharmaceutical Industry:
Phenol, 2,6-bis[[2-[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]phenyl]methyl]-4-nitroserves as a key component in the synthesis of certain pharmaceuticals. Its unique structure allows for the development of drugs with specific therapeutic properties, such as anti-inflammatory or analgesic effects.
Used in Chemical Synthesis:
The presence of the nitro group in the molecule makes Phenol, 2,6-bis[[2-[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]phenyl]methyl]-4-nitroa valuable precursor in the synthesis of other organic compounds. It can be used to produce a variety of chemical intermediates, which are essential in the manufacture of dyes, pesticides, and other specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 137794-34-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,7,9 and 4 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 137794-34:
(8*1)+(7*3)+(6*7)+(5*7)+(4*9)+(3*4)+(2*3)+(1*4)=164
164 % 10 = 4
So 137794-34-4 is a valid CAS Registry Number.
137794-34-4Relevant academic research and scientific papers
New Crown Ether-like Macrocycles Containing a Nitrophenol Unit. Synthesis and Metal Ion Effects on the Reactivity of Their Acetates in Transacylation Reactions
Kraft, Dagmar,Cacciapaglia, Roberta,Boehmer, Volker,El-Fadl, A. Abu,Haekema, Sybolt,et al.
, p. 826 - 834 (2007/10/02)
A series of crown ether-like macrocyclic compounds 3 containing the 2,6-dibenzyl-4-nitrophenol structure have been prepared by cyclization reactions of disalicylideneacetone 4 with ditosylates 7 of oligoethylene glycols, followed by hydrogenation and double aldol condensation with nitromalondialdehyde.These compounds may be regarded as possessing a section of a 1,3-crowned calixarene.X-ray analysis of two examples shows, however, that the three phenolic units linked via o-methylene groups adopt a conformation different to the all-cis conformation found in calixarenes.The reaction of the nitrophenyl acetates derived from 3 and from suitable model compounds with ethoxide in ethanol was studied kinetically.This reaction is accelerated by the addition of SrBr2 and BaBr2 in all cases, indicating that the metal ion is bound more strongly to the transition state than to the initial state.Especially high acceleration factors (up to 700 in the case of 10e) were observed for cyclic and open-chain compounds with longer flexible oligoethylene oxide chains, which means that only in these cases do the ether oxygens contribute effectively to the binding of the metal ion in the transition state.
