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9(10H)-Acridinone, 10-[4-(1,1-dimethylethyl)phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

104014-67-7

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104014-67-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104014-67-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,0,1 and 4 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 104014-67:
(8*1)+(7*0)+(6*4)+(5*0)+(4*1)+(3*4)+(2*6)+(1*7)=67
67 % 10 = 7
So 104014-67-7 is a valid CAS Registry Number.

104014-67-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 10-(4-tert-Butylphenyl)-9(10H)-acridinon

1.2 Other means of identification

Product number -
Other names 10-(4-tert-Butyl-phenyl)-10H-acridin-9-one

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:104014-67-7 SDS

104014-67-7Downstream Products

104014-67-7Relevant academic research and scientific papers

Copper-catalyzed synthesis of N-aryl acridones from 2-amino benzophenones and aryl boronic acids via sequential double oxidative C–N coupling

He, Yang,Xu, Liang,Zhang, Jinli,Wei, Yu

, (2019/12/27)

Pot-economic synthesis of N-aryl acridones was performed with 2-aminobenzophenones and aryl boronic acids as starting materials. Cu-catalyzed chelation-assisted oxidative C–N cross-coupling reactions were well merged with the following intra-molecular oxidative dehydrogenative C–H amination reactions under an air atmosphere. The use of reagent capsules can further resolve the compatibility problem of reagents and simplify the operational process, providing a more straightforward access to the target products.

Synthesis and physical properties of π-extended molecules having p-methylenequinone unit

Umeda, Rui,Nakatsukasa, Masamichi,Nishiyama, Yutaka

, p. 318 - 327 (2020/01/31)

In this paper, we reported the facile synthesis of the π-extended molecules having p-methylenequinone unit from the aromatic ketones, such as fluorenone, xanthone, thioxanthone, dibenzosuberenone, and acridone, in few steps and the results of their physic

Synthesis of Acridones by Palladium-Catalyzed Buchwald-Hartwig Amination

Janke, Julia,Villinger, Alexander,Ehlers, Peter,Langer, Peter

, p. 817 - 820 (2019/04/25)

The Buchwald-Hartwig amination allows an efficient and convenient synthesis of biologically and pharmaceutically important acridones by formation of a six-membered ring. With the described method, a number of derivatives have been synthesized in up to 95% yield by using a variety of anilines as well as benzylic and aliphatic amines.

12-Organyldibenzazocine-5,7-diones

Hellwinkel, Dieter,Ittemann, Peter

, p. 3165 - 3197 (2007/10/02)

The title compounds 10, 23 are formed in low yields on treatment of 2,2'-organylimino-bisbenzoic acid esters 8 with methyllithium, but in high yields in the intramolecular ester condensation with sodium hydride of triarylamines 12, containing o-acetyl-, a

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