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134859-18-0

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134859-18-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 134859-18-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,8,5 and 9 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 134859-18:
(8*1)+(7*3)+(6*4)+(5*8)+(4*5)+(3*9)+(2*1)+(1*8)=150
150 % 10 = 0
So 134859-18-0 is a valid CAS Registry Number.

134859-18-0Downstream Products

134859-18-0Relevant articles and documents

Poly(N,N ′-dibromo-N-ethyl-benzene-1,3-disulphonamide) and N,N,N ′,N ′-tetrabromobenzene-1,3- disulphonamide as novel catalysts for synthesis of quinoxaline derivatives

Ghorbani-Vaghei, Ramin,Hajinazari, Somaye

, p. 353 - 358 (2013)

Poly(N,N ′ -dibromo-N-ethyl-benzene-1,3-disulphonamide) [PBBS] and N,N,N ′,N ′ -tetrabromobenzene-1,3- disulphonamide [TBBDA] were used as efficient catalysts for the synthesis of quinoxaline derivatives in excellent yields from 1,2-diamines and 1,2-dicarbonyls under aqueous and solvent-free conditions. [Figure not available: see fulltext.]

Zirconium triflate: An efficient catalyst for the synthesis of quinolines and quinoxalines

Kolvari, Eskandar,Zolfigol, Mohammad Ali,Koukabi, Nadiya,Gilandust, Maryam,Kordi, Abdol-Vahid

, p. 1183 - 1191 (2013/11/06)

An environmentally friendly method is described for the preparation of substituted quinoline and quinoxaline derivatives using Zr(OTf)4 as an efficient catalyst. The method is based on using 1,3-diketones, ketones and 2-aminoaryl ketones under solvent-free conditions and also on using 1,2-diketone, 1,2-diamine in EtOH/H2O at room temperature for quinloine and quinoxaline synthesis, respectively. The advantages in using this method, include its environmental friendliness, simple operating process and good yields.

A modified synthesis of some novel polycyclic aromatic phenazines and quinoxalines by using the tungstate sulfuric acid (TSA) as a reusable catalyst under solvent-free conditions

Karami, Bahador,Khodabakhshi, Saeed,Nikrooz, Marzieh

experimental part, p. 187 - 192 (2012/07/16)

Considering the synthesis of new compounds, we developed heterocyclic chemistry. We also helped to improve the classical synthetic route for the synthesis of quinoxalines and phenazines through implement in terms of solvent-free reaction. For the condensa

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