52322-81-3 Usage
Description
1-(CHLOROMTHYL)-3-PHENOXY BENZENE, also known as 1-(chloromethyl)-3-phenoxybenzene, is a chemical compound with the molecular formula C13H11ClO. It is a chlorinated derivative of 3-phenoxybenzene, characterized by its white solid appearance, solubility in organic solvents, and a slightly aromatic odor. Due to its moderately toxic nature, it should be handled with caution. The presence of the chloromethyl group in its structure makes it a valuable building block in organic synthesis reactions, particularly in the pharmaceutical and agrochemical industries.
Uses
Used in Pharmaceutical Industry:
1-(CHLOROMTHYL)-3-PHENOXY BENZENE is used as a precursor for the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
1-(CHLOROMTHYL)-3-PHENOXY BENZENE is also used as a starting material in the synthesis of agrochemicals, such as pesticides and herbicides. Its versatility in organic synthesis reactions enables the creation of effective compounds for agricultural use.
Check Digit Verification of cas no
The CAS Registry Mumber 52322-81-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,3,2 and 2 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 52322-81:
(7*5)+(6*2)+(5*3)+(4*2)+(3*2)+(2*8)+(1*1)=93
93 % 10 = 3
So 52322-81-3 is a valid CAS Registry Number.
52322-81-3Relevant articles and documents
Copper(II) trans-bis-(glycinato): An efficient heterogeneous catalyst for cross coupling of phenols with aryl halides
Verma, Sanny,Kumar, Neeraj,Jain, Suman L.
experimental part, p. 4665 - 4668 (2012/09/05)
Copper(II) trans-bis-(glycinato) complex, easily prepared by the solid state reaction of copper(II) acetate and glycine (trans-[Cu(glyo) 2·H2O]) was found to be an efficient, recyclable, and high yielding catalyst for the Ullmann type synthesis of diaryl ethers via the cross coupling of phenols with aryl halides without using any additives at relatively low reaction temperature. The catalyst could easily be recovered by simple filtration and was reused for several runs with consistent catalytic activity.