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4H-1-Benzopyran-4-one,2-amino-3-phenyl-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79429-63-3

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79429-63-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79429-63-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,4,2 and 9 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 79429-63:
(7*7)+(6*9)+(5*4)+(4*2)+(3*9)+(2*6)+(1*3)=173
173 % 10 = 3
So 79429-63-3 is a valid CAS Registry Number.

79429-63-3SDS

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 2-amino-3-phenylchromen-4-one

1.2 Other means of identification

Product number -
Other names 2-amino-3-phenyl-4H-chromen-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:79429-63-3 SDS

79429-63-3Downstream Products

79429-63-3Relevant academic research and scientific papers

Synthesis of chromeno[2,3-b ]indol-11(6 H)-one via PhI(OAc)2-mediated intramolecular oxidative C(sp2)-N(H2) bond formation

Sun, Jiyun,Zhang-Negrerie, Daisy,Du, Yunfei,Zhao, Kang

, p. 1200 - 1206 (2015)

Various chromeno[2,3-b]indol-11(6H)-ones were conveniently constructed via phenyliodine(III) diacetate (PIDA)-mediated intramolecular oxidative annulation. This method, while realizing a direct oxidative C-N bond formation between an aromatic ring and a p

Flavones and structurally related 4-chromenones inhibit carbonic anhydrases by a different mechanism of action compared to coumarins

Balboni, Gianfranco,Congiu, Cenzo,Onnis, Valentina,Maresca, Alfonso,Scozzafava, Andrea,Winum, Jean-Yves,Maietti, Annalisa,Supuran, Claudiu T.

experimental part, p. 3063 - 3066 (2012/06/17)

An inhibition study of several carbonic anhydrase (CA, EC 4.2.1.1) isoforms with flavones and aminoflavones, compounds possessing a rather similar scaffold with the coumarins, recently discovered inhibitors of this enzyme, is reported. The natural product

Convenient synthesis of chromones and quinolinones

Hemavathi,Naveen,Lokanatha Rai

, p. 409 - 410 (2013/09/24)

A one pot synthesis of substituted chromones and quinolinones by condensing commercially available and cheaper molecules like salicylic acid and anthranilic acid respectively with alkenes / nitriles followed by insitu cyclization using ammonium acetate as base has been achieved.

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