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2-(4-iodophenyl)-4H-chromen-4-one is a chemical compound with the molecular formula C14H9IO2. It is a derivative of the flavone class of compounds, characterized by a benzopyrone structure with a phenyl ring at the 2-position and an iodine atom at the 4-position of the phenyl ring. 2-(4-iodophenyl)-4H-chromen-4-one is known for its potential applications in the field of organic synthesis and as a building block for the development of pharmaceuticals and other chemical products. It is also of interest in research due to its structural properties and the possibility of its involvement in various chemical reactions. The presence of the iodine atom makes it a candidate for reactions involving halogenation or as a precursor for further functionalization.

1026-44-4

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1026-44-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1026-44-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,2 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1026-44:
(6*1)+(5*0)+(4*2)+(3*6)+(2*4)+(1*4)=44
44 % 10 = 4
So 1026-44-4 is a valid CAS Registry Number.

1026-44-4SDS

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-iodophenyl)chromen-4-one

1.2 Other means of identification

Product number -
Other names 4'-Iodoflavanone

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:1026-44-4 SDS

1026-44-4Downstream Products

1026-44-4Relevant academic research and scientific papers

Use of [125I]4'-iodoflavone as a tool to characterize ligand-dependent differences in Ah receptor behavior.

Swanson, Hollie I,Whitelaw, Murray L,Petrulis, John R,Perdew, Gary H

, p. 298 - 310 (2002)

We have synthesized [(125)I]4'-iodoflavone to study Ah receptor (AhR)-ligand interactions by a class of AhR ligands distinct from the prototypic ligand 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD). This radioligand allows the comparison of AhR-ligand intera

Divergent synthesis of flavones and flavanones from 2′-hydroxydihydrochalconesviapalladium(ii)-catalyzed oxidative cyclization

Son, Seung Hwan,Cho, Yang Yil,Yoo, Hyung-Seok,Lee, Soo Jin,Kim, Young Min,Jang, Hyu Jeong,Kim, Dong Hwan,Shin, Jeong-Won,Kim, Nam-Jung

, p. 14000 - 14006 (2021/04/22)

Divergent and versatile synthetic routes to flavones and flavanonesviaefficient Pd(ii) catalysis are disclosed. These Pd(ii) catalyses expediently provide a variety of flavones and flavanones from 2′-hydroxydihydrochalcones as common intermediates, depending on oxidants and additives,viadiscriminate oxidative cyclization sequences involving dehydrogenation, respectively, in a highly atom-economic manner.

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