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3,3'-Dimethoxy-benzoinacetat, also known as 3,3'-dimethoxybenzoin acetate, is an organic compound with the chemical formula C17H18O5. It is a derivative of benzoin, featuring two methoxy groups attached to the benzene rings and an acetate group. 3,3'-Dimethoxy-benzoinacetat is primarily used as a synthetic intermediate in the production of various pharmaceuticals, agrochemicals, and other specialty chemicals. Its structure provides unique reactivity and properties, making it a valuable building block in organic synthesis. The compound is typically synthesized through the condensation of salicylaldehyde with an appropriate acetate, followed by methylation. Due to its reactivity, 3,3'-dimethoxy-benzoinacetat is often employed in the preparation of complex molecules and has applications in the fields of chemistry, biology, and materials science.

2188-17-2

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2188-17-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2188-17-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,8 and 8 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2188-17:
(6*2)+(5*1)+(4*8)+(3*8)+(2*1)+(1*7)=82
82 % 10 = 2
So 2188-17-2 is a valid CAS Registry Number.

2188-17-2Downstream Products

2188-17-2Relevant academic research and scientific papers

Selective Synthesis of Acylated Cross-Benzoins from Acylals and Aldehydes via N-Heterocyclic Carbene Catalysis

Onodera, Kou,Suzuki, Yumiko,Takashima, Ryo

, p. 4197 - 4202 (2021/06/27)

The utility of acylals as building blocks for selective cross-benzoin synthesis was explored in this study. The synthesis of α-acetoxyketones (O-acyl cross-benzoins) was achieved via selective N-heterocyclic carbene-catalyzed cross-benzoin reactions using acylals as aldehyde equivalents. Thus, the combination of ortho-substituted phenyl acylals and aromatic/aliphatic aldehydes as coupling substrates using bicyclic triazolium salts as precatalysts and potassium carbonate as a base in THF at reflux temperature selectively yielded O-acyl cross-benzoins.

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