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1-(tert-butyl)-2-benzyl azodicarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

883306-83-0

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883306-83-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 883306-83-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,3,3,0 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 883306-83:
(8*8)+(7*8)+(6*3)+(5*3)+(4*0)+(3*6)+(2*8)+(1*3)=190
190 % 10 = 0
So 883306-83-0 is a valid CAS Registry Number.

883306-83-0Relevant academic research and scientific papers

Synthesis and application of a novel asymmetric azo reagent: 1-(tert-butyl)-2-(4-chlorobenzyl) azodicarboxylate (tBCAD)

Xie, Jian,Xu, Cai,Dai, Qianjin,Wang, Xiaozhong,Xu, Gang,Chen, Yingqi,Dai, Liyan

, p. 5321 - 5326 (2017/08/04)

A series of novel asymmetric azo reagents, 1-(tert-butyl)-2-(4-substituted benzyl) azodicarboxylate, were prepared. The synthetic process has the advantage of simpleness, easy operation, mild reaction condition and high yield. The 1-(tert-butyl)-2-(4-chlorobenzyl) azodicarboxylate (tBCAD) was selected for its stability and convenience to handle, and its precursor can be recycled by recrystallization with toluene. The tBCAD and DIAD were applied to a wide variety of Mitsunobu reactions. The experimental results showed that the performance of tBCAD in Mitsunobu reaction was comparable to that of DIAD, while the stability of tBCAD was much better than DIAD. Thus, tBCAD can be a novel, stable, effective azo-reagent for the Mitsunobu reaction.

Cyclic dibenzoylhydrazines reproducing the conformation of ecdysone agonists, RH-5849

Toya, Tetsuya,Yamaguchi, Kentaro,Endo, Yasuyuki

, p. 953 - 961 (2007/10/03)

We have investigated the biologically active conformation of the non-steroidal ecdysone agonist, 1-tert-butyl-1,2-dibenzoylhydrazine (RH-5849) by means of design, synthesis and conformational analysis of cyclic derivatives of RH-5849. Among the synthesize

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