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2-p-Toluolsulfonylamino-2'-methoxy-benzophenon is a complex organic compound with the chemical formula C19H17NO4S. It is a derivative of benzophenone, featuring a p-toluolsulfonylamino group attached to one benzene ring and a methoxy group on the other. 2-p-Toluolsulfonylamino-2'-methoxy-benzophenon is known for its potential applications in the synthesis of various pharmaceuticals and organic compounds due to its unique structure and reactivity. It is typically used as an intermediate in chemical reactions, particularly in the preparation of dyes and other specialty chemicals. The compound's properties, such as its solubility and stability, make it a valuable component in advanced chemical research and industrial processes.

1823-21-8

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1823-21-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1823-21-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,2 and 3 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1823-21:
(6*1)+(5*8)+(4*2)+(3*3)+(2*2)+(1*1)=68
68 % 10 = 8
So 1823-21-8 is a valid CAS Registry Number.

1823-21-8Downstream Products

1823-21-8Relevant articles and documents

Diastereo- And Atroposelective Synthesis of Bridged Biaryls Bearing an Eight-Membered Lactone through an Organocatalytic Cascade

Lu, Shenci,Ong, Jun-Yang,Yang, Hui,Poh, Si Bei,Liew, Xi,Seow, Chwee San Deborah,Wong, Ming Wah,Zhao, Yu

, p. 17062 - 17067 (2019)

We present herein an unprecedented stereoselective synthesis of bridged biaryls with defined axial and central chirality from readily available starting materials. This N-heterocyclic carbene-catalyzed method proceeds through propargylic substitution of azolium enolates followed by two-directional cyclization, as supported by DFT calculation. A range of benzofuran/indole-derived bridged biaryls bearing an eight-membered lactone are accessed with uniformly high stereoselectivity (>98:2 dr, mostly >98% ee).

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