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4-[(2-phenylethyl)amino]-2H-chromen-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

111222-28-7

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111222-28-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 111222-28-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,2,2 and 2 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 111222-28:
(8*1)+(7*1)+(6*1)+(5*2)+(4*2)+(3*2)+(2*2)+(1*8)=57
57 % 10 = 7
So 111222-28-7 is a valid CAS Registry Number.

111222-28-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(2-phenylethylamino)chromen-2-one

1.2 Other means of identification

Product number -
Other names 4-phenethylaminocoumarin

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:111222-28-7 SDS

111222-28-7Relevant articles and documents

Synthesis, structure, and estrogenic activity of 4-amino-3-(2-methylbenzyl)coumarins on human breast carcinoma cells

Jacquot, Yves,Laios, Ioanna,Cleeren, Anny,Nonclercq, Denis,Bermont, Laurent,Refouvelet, Bernard,Boubekeur, Kamal,Xicluna, Alain,Leclercq, Guy,Laurent, Guy

, p. 2269 - 2282 (2007)

A number of coumarins exhibit interesting pharmacological activities and are therefore of therapeutic use. We report here the synthesis and the structural analysis of new N-substituted 4-amino-3-(2-methylbenzyl)coumarins (compounds 8a-8e) that present str

Synthesis and Photophysical Properties of 1,4-Dihydro-2 H,5H-chromeno[4,3-D][1,3]oxazin-5-ones, and Derivatives Containing Tethered 1,2,3-Triazoles, from 4-Aminocoumarins

Brites, Nathan P.,Dilelio, Marina C.,Iglesias, Bernardo A.,Kaufman, Teodoro S.,Silveira, Claudio C.,Vieira, Larissa A.

, p. 2965 - 2976 (2019/07/22)

A facile protocol for the unprecedented one-pot H 2 SO 4 -mediated hydroxymethylation/cyclative N, O -acetalization of 4-aminocoumarins to 1,4-dihydro-2 H,5 H -chromeno[4,3- d ][1,3]oxazin-5-ones, in moderate to good yields, was deve

Microwave assisted synthesis of 4-aryl/alkylaminocoumarins

Chavan, Abhijit P.

, p. 179 - 181 (2007/10/03)

4-Aryl and 4-alkylaminocoumarins were prepared by reaction of 4-hydroxycoumarin with amines under microwave irradiation in solvent-free conditions in good to excellent yields.

A Novel Transformation of 4-Arylaminocoumarins to 6H-1-Benzopyranoquinolin-6-ones Under Vilsmeier-Haack Conditions

Tabakovic, K.,Tabakovic, I.,Ajdini, N.,Leci, O.

, p. 308 - 310 (2007/10/02)

4-Aryl and 4-alkylaminocoumarins 1 were prepared by reacting of 4-hydroxycoumarin and an appropriate amine.The reaction of 1 with phosphorousoxychloride/dimethylformamide led to 6H-1-benzopyranoquinoline-6-one derivatives 2 in very good yields, whi

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