25562-89-4 Usage
Uses
Used in Pharmaceutical Industry:
[2-(4-METHYLPHENOXY)PHENYL]METHANOL is used as an intermediate in the synthesis of pharmaceuticals for its versatile chemical properties, contributing to the development of various medications.
Used in Agricultural Chemicals Industry:
In the agricultural chemicals industry, [2-(4-METHYLPHENOXY)PHENYL]METHANOL is utilized as an intermediate, playing a crucial role in the production of different agrochemicals that aid in enhancing crop protection and yield.
Used in Plasticizers Production:
[2-(4-METHYLPHENOXY)PHENYL]METHANOL is used as a raw material for the production of plasticizers, which are additives that increase the flexibility and workability of plastics, making them more suitable for various applications.
Used in Lubricants Production:
[2-(4-METHYLPHENOXY)PHENYL]METHANOL is also employed as a raw material in the production of lubricants, which are essential for reducing friction between moving parts in various mechanical systems, thus enhancing their performance and longevity.
Used in Other Industrial Chemicals Production:
[2-(4-METHYLPHENOXY)PHENYL]METHANOL finds application as a raw material in the manufacturing of other industrial chemicals, showcasing its versatility and importance in the chemical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 25562-89-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,5,6 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 25562-89:
(7*2)+(6*5)+(5*5)+(4*6)+(3*2)+(2*8)+(1*9)=124
124 % 10 = 4
So 25562-89-4 is a valid CAS Registry Number.
25562-89-4Relevant academic research and scientific papers
Gas-phase Reactions of 2-Benzyl- and 2-Benzoyl-phenoxyl Radicals, and of 2-Phenoxybenzyl Radicals: Examples of New Hydrogen-transfer Processes
Cadogan, J. I. G.,Hutchison, H. Susan,McNab, Hamish
, p. 385 - 393 (2007/10/02)
Generation of the 2-benzylphenoxyl radical 23 or the 2-phenoxybenzyl radical 24 by flash vacuum pyrolysis of the ethers 8 or 9, or the oxalate 19, respectively, leads to fluoren-1-ol 22 together with 2-benzylphenol 7 and a low yield of xanthene 21.Pyrolysis of the para-substituted derivatives 11 and 20 gives an analogous distribution of products, including two isomeric methylxanthenes 28 and 29 formed via the spirodienyl 27.The reactions of the corresponding 2-benzoylphenoxyl radicals give information on the mechanism of these processes.Thus the formation of the fluorenones 37 and 43 provides evidence for the hydrogen-abstraction mechanism (Scheme 4) of fluorene formation.Secondly, a detailed study of the ratios of xanthones 41 and 42 under a variety of pyrolysis conditions suggests that such 6-membered-ring products are formed by sigmatropic shifts in the spirodienyl, rather than direct cyclisation of the phenoxyl or benzoyl radicals.
