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β-(3,5-Dimethoxyphenyl)ethanesulfonyl azide is a chemical compound with the molecular formula C10H13N3O5S. It is a derivative of ethanesulfonyl azide, featuring a 3,5-dimethoxyphenyl group attached to the β-carbon. β-(3,5-Dimethoxyphenyl)ethanesulfonyl azide is known for its reactivity and is often used in chemical synthesis, particularly in the preparation of various pharmaceuticals and agrochemicals. Its structure allows for the formation of diverse products through reactions such as cyclizations and rearrangements, making it a valuable intermediate in organic chemistry. The compound's properties, including its potential reactivity with nucleophiles and electrophiles, are of interest to researchers in the field of chemical synthesis.

88106-84-7

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88106-84-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88106-84-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,1,0 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 88106-84:
(7*8)+(6*8)+(5*1)+(4*0)+(3*6)+(2*8)+(1*4)=147
147 % 10 = 7
So 88106-84-7 is a valid CAS Registry Number.

88106-84-7Relevant academic research and scientific papers

Thermolysis of Sulfonyl Azides Bearing Nucleophilic Neighboring Groups. A Search for Anchimeric Assistance

McManus, Samuel P.,Smith, Maurice R.,Abramovitch, Rudolph A.,Offor, Mercy N.

, p. 683 - 687 (2007/10/02)

In a search for anchimeric assistance by n- or ?-donor neighboring groups in sulfonyl azide decompositions, 25 sulfonyl azides have been prepared and thermolyzed in 1-chloronaphthalene.First-order rate constants at 135 and 165 deg C were determined by mea

Solution and Flash Vacuum Pyrolyses of β-(3,5-Disubstituted-phenyl)ethanesulfonyl Azides. Sultam, Pyrindine, and Azepine Formation

Abramovitch, Rudolph A.,Holcomb, William D.,Thompson, W. Marshall,Wake, Shigeo

, p. 5124 - 5131 (2007/10/02)

The solution and flash vacuum pyrolyses of β-(3,5-disubstituted-phenyl)ethanesulfonyl azides are reported.When R = Me, FVP results suggest that the substituents stabilize the intermediate leading to the 3,4-dihydro-2,1-benzothiazepine 2,2-dioxide (6a).A n

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