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Benzoic acid, 2-[(2,3-dihydro-1,4-benzodioxin-6-yl)amino]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

154490-83-2

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154490-83-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 154490-83-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,4,9 and 0 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 154490-83:
(8*1)+(7*5)+(6*4)+(5*4)+(4*9)+(3*0)+(2*8)+(1*3)=142
142 % 10 = 2
So 154490-83-2 is a valid CAS Registry Number.

154490-83-2Downstream Products

154490-83-2Relevant academic research and scientific papers

Synthesis and?biological evaluation of?modified acridines: the?effect of?N- and?O- substituent in?the?nitrogenated ring on?antitumor activity

Sánchez, Isabel,Reches, Rosa,Caignard, Daniel Henry,Renard, Pierre,Pujol, Maria Dolors

, p. 340 - 352 (2007/10/03)

A series of new acridines has been prepared by cyclodehydration of N-(2,3-dihydro-1,4-benzodioxin-6-yl)anthranilic acid in acidic media following classical procedures. All these compounds have in common a dioxygenated ring fused to the acridine. The tetra

Ultrasonic irradiation of the Ullmann condensation: Application to the preparation of dioxolo, dioxino, cyclopent, and imidazolo anthranilic acid derivatives

Robin, Maxime,Pique, Valerie,Faure, Robert,Galy, Jean-Pierre

, p. 1083 - 1085 (2007/10/03)

The synthesis of N-aryl anthranilic acid derivatives bearing dioxolo, dioxino, cyclopent, and imidazolo supplementary ring systems is reported. The Ullmann-Goldberg condensation of the N-aryl anthranilic acid is improved in yield and reaction time, compar

Synthesis of new n-alkyl- and n-acyldioxinophenothiazine and acridinone derivatives

Chatel, Florence,Morel, Sandrine,Boyer, Gérard,Galy, Jean Pierre

, p. 2535 - 2552 (2007/10/03)

The synthesis of new substituted dioxino[b]- and [c]phenothiazines or acridinones is reported. N-Arylation of [1,4]benzodioxin-6-amine with organolead or organobismuth reagents gave N-aryl-2,3-dihydro-1,4-benzodioxin-6-amine; subsequent Bernthsen thionati

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