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Hydrazinecarboxylic acid, 2,2',2''-(1,3,5-benzenetriyl)tris[1-phenyl-, tris(1,1-dimethylethyl) ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

681815-36-1

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681815-36-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 681815-36-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,1,8,1 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 681815-36:
(8*6)+(7*8)+(6*1)+(5*8)+(4*1)+(3*5)+(2*3)+(1*6)=181
181 % 10 = 1
So 681815-36-1 is a valid CAS Registry Number.

681815-36-1Downstream Products

681815-36-1Relevant academic research and scientific papers

Synthesis of Novel 1,3,5-Tris(arylazo)benzenes via Pd-Catalyzed Couplings and Cu(I)-Mediated Direct Oxidations

Lim, Young-Kwan,Choi, Sunju,Park, Kyung Bae,Cho, Cheon-Gyu

, p. 2603 - 2606 (2004)

A series of novel 1,3,5-tris-azobenzenes were prepared from 1,3,5-trihalobenzene via Pd-catalyzed couplings of N-Boc aryl hydrazines and subsequent Cu(I)-mediated direct oxidations. The oxidation of tris-arylhydrazide provided the azobenzene as a mixture

Regioselective [5,5]-sigmatropic rearrangement reactions of aryl hydrazides

Kang, Hong-Min,Lim, Young-Kwan,Shin, In-Jee,Kim, Hee-Yeon,Cho, Cheon-Gyu

, p. 2047 - 2050 (2007/10/03)

N,N′-Aryl hydrazides with substituents at the ortho or meta positions undergo highly regioselective [5,5]-sigmatropic rearrangement reactions to furnish benzidines in good to excellent isolated yields. The presence of single substituent at either the ortho or meta position provides sufficient bias, effectively suppressing the formation of diphenylene, the major byproduct of the conventional benzidine rearrangement reaction.

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