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β-(3-Methyl-4-chlorophenoxy)-acetophenon, also known as 2-(3-methyl-4-chlorophenoxy)-1-phenylethanone, is an organic compound with the chemical formula C15H13ClO2. It is a derivative of acetophenone, featuring a 3-methyl-4-chlorophenoxy group attached to the β-position of the acetophenone molecule. β-<3-Methyl-4-chlor-phenoxy>-acetophenon is characterized by its aromatic structure, which includes a chlorine atom at the para position and a methyl group at the ortho position on the phenoxy ring. It is a colorless to pale yellow solid and is used in the synthesis of various pharmaceuticals and agrochemicals due to its potential biological activity. The compound's properties, such as its melting point, solubility, and reactivity, can be influenced by the presence of the chlorine and methyl substituents, making it a versatile intermediate in organic synthesis.

20895-59-4

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20895-59-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20895-59-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,8,9 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 20895-59:
(7*2)+(6*0)+(5*8)+(4*9)+(3*5)+(2*5)+(1*9)=124
124 % 10 = 4
So 20895-59-4 is a valid CAS Registry Number.

20895-59-4Downstream Products

20895-59-4Relevant academic research and scientific papers

Use of a scientific microwave apparatus for rapid optimization of reaction conditions in a monomode function and then substrate screening in a multimode function

Leadbeater, Nicholas E.,Schmink, Jason R.

, p. 6764 - 6773 (2007)

Recently, a new apparatus has become available, which aims to bring together in one unit the advantages of a monomode and a multimode microwave device. We have assessed the applicability of the apparatus toward rapid optimization of reaction conditions in a monomode function and then substrate screening in a multimode function. We have also probed the effects of differences in microwave absorptivity of reaction mixtures on the product conversions in screening multiple substrates simultaneously in a multimode microwave apparatus. We find that when the microwave absorptivity of a reaction mixture is dictated by the solvent, there is little effect on the heating profile of varying the substrate in a screening run. However, this is not the case when reactions involving non-microwave absorbant solvents are used. In this case the characteristics of the substrate can affect significantly the outcome of the reaction.

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