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4H-3,1-Benzoxazin-4-one, 2-[4-(dimethylamino)phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

95654-38-9

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95654-38-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95654-38-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,6,5 and 4 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 95654-38:
(7*9)+(6*5)+(5*6)+(4*5)+(3*4)+(2*3)+(1*8)=169
169 % 10 = 9
So 95654-38-9 is a valid CAS Registry Number.

95654-38-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[4-(dimethylamino)phenyl]-3,1-benzoxazin-4-one

1.2 Other means of identification

Product number -
Other names 2-(4-dimethylaminophenyl)-4H-benzo[d][1,3]oxazin-4-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:95654-38-9 SDS

95654-38-9Downstream Products

95654-38-9Relevant academic research and scientific papers

Rhodium(iii)-catalyzed cascade reactions of benzoic acids with dioxazolones: Discovery of 2,5-substituted benzoxazinones as AIE molecules

Li, Jinbiao,Zhang, Shuaizhong,Lonka, Madhava Reddy,Zhang, Jinquan,Zou, Hongbin

, p. 11203 - 11206 (2019/09/30)

A rhodium-catalyzed cascade reaction of benzoic acids with 1,4,2-dioxazol-5-ones was studied. The carboxyl group enabled a double C-H amidation followed by further intramolecular cyclization to afford 2,5-substituted benzoxazinones, which exhibited aggregation-induced emission (AIE) properties with a promising excited-state intramolecular proton-transfer (ESIPT) phenomenon.

Silver and Palladium Cocatalyzed Carbonylative Activation of Benzotriazoles to Benzoxazinones under Neutral Conditions

Yin, Zhiping,Wang, Zechao,Wu, Xiao-Feng

supporting information, p. 6232 - 6235 (2017/11/24)

A novel and efficient method for the carbonylative activation of benzotriazoles to benzoxazinones has been developed. By using a silver and palladium bimetallic catalyst system, a broad range of benzotriazoles were transformed into the corresponding benzoxazinones in moderate to good yields with excellent functional group tolerance. Notably, this procedure proceeds under neutral conditions.

A convenient and general palladium-catalyzed carbonylative coupling for the synthesis of 2-arylbenzoxazinones

Wu, Xiao-Feng,Schranck, Johannes,Neumann, Helfried,Beller, Matthias

supporting information; experimental part, p. 12246 - 12249 (2011/12/02)

CO and CO again: A new double carbonylation methodology for the synthesis of 2-arylbenzoxazinones has been developed (see scheme). Copyright

Studies on Quinazolinones as Dual Inhibitors of Pgp and MRP1 in Multidrug Resistance

Wang, Shouming,Ryder, Hamish,Pretswell, Ian,Depledge, Paul,Milton, John,Hancox, Timothy C.,Dale, Ian,Dangerfield, Wendy,Charlton, Peter,Faint, Richard,Dodd, Rory,Hassan, Stephanie

, p. 571 - 574 (2007/10/03)

The syntheses and SAR studies of various quinazolinone compounds are described for the dual inhibition of Pgp and MRP1 in multidrug resistance.

Nukleophile Reaktionen an 2-Phenylindolenin-3-onen

Adam, Jean-Marie,Winkler, Tammo

, p. 2186 - 2191 (2007/10/02)

Nucleophilic reagents such as 4-nitrophenylhydrazine, malonic acid derivatives, and hydrogen peroxide react with 2-phenylindolenin-3-ones giving, in the first step, addition products to the N=C(2) bond.This addition can be reversible, but in most cases ne

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