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ω-Chloro-2-hydroxy-6-methoxyacetophenone is an organic compound with the chemical formula C9H9ClO3. It is a derivative of acetophenone, featuring a chloro group at the omega position, a hydroxy group at the 2nd position, and a methoxy group at the 6th position on the benzene ring. ω-Chloro-2-hydroxy-6-methoxyacetophenone is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as an intermediate in the production of certain drugs and pesticides. Its chemical structure endows it with reactivity that can be harnessed in organic synthesis, making it a valuable component in the development of new chemical entities.

75717-59-8

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75717-59-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75717-59-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,7,1 and 7 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 75717-59:
(7*7)+(6*5)+(5*7)+(4*1)+(3*7)+(2*5)+(1*9)=158
158 % 10 = 8
So 75717-59-8 is a valid CAS Registry Number.

75717-59-8Downstream Products

75717-59-8Relevant academic research and scientific papers

Ortho-Coordinated Acylation on Phenol Systems

Sartori, Giovanni,Casnati, Giuseppe,Bigi, Franca

, p. 4371 - 4377 (2007/10/02)

The ortho-coordinated acylation of phenol salts reported in recent synthetic applications has been extensively investigated.The data obtained support the hypothesis that formation of an organized complex between the phenol salts and the acylating agents may strongly influence the reaction pathway, depending on the nature of the specific cation, phenol, and acyl chloride involved in the process.The structural factors which control the formation of the reacting complex 3 have been extensively investigated; the results obtained allow us to discuss the possibilities and limitations of this methodology in selective o-acylphenol synthesis.The present methodology is the procedure of choice for ortho-functionalization of phenols with electrophilic reagents such as phosgene, oxaloyl chlorides, polyunsaturated acid chlorides, phthalic dichlorides, and, in general, acid chlorides α-functionalized with an electron-withdrawing group.

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