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

118092-39-0

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118092-39-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 118092-39-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,0,9 and 2 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 118092-39:
(8*1)+(7*1)+(6*8)+(5*0)+(4*9)+(3*2)+(2*3)+(1*9)=120
120 % 10 = 0
So 118092-39-0 is a valid CAS Registry Number.

118092-39-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(bromomethyl)-2-phenylchromen-4-one

1.2 Other means of identification

Product number -
Other names 3-Brommethylflavon

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:118092-39-0 SDS

118092-39-0Relevant academic research and scientific papers

SUBSTITUTED PYRIMIDINE COMPOUNDS AS PHOSPHATIDYLINOSITOL 3-KINASE DELTA INHIBITOR AND USE THEREOF

-

, (2018/02/03)

The present invention belongs to the field of medicinal chemistry, and relates to substituted pyrimidine compounds as phosphatidylinositol 3-kinase (PI3K) δ inhibitor and a use thereof. In particular, the present invention provides a compound as shown by formula I or an isomer, pharmaceutically acceptable salt, solvate or prodrug thereof, the preparation methods of same and pharmaceutical compositions containing these compounds and a use of these compounds or compositions for treating cancer, hyperblastosis diseases or inflammatory diseases. The compounds of the present invention have a good inhibiting activity on PI3Kδ and have a high selectivity. It is hoped that these will be therapeutic agents for cancer, hyperblastosis diseases or inflammatory diseases.

One-pot synthesis of 3-methylflavones and their transformation into (E)-3-styrylflavones via Wittig reactions

Rocha, Djenisa H. A.,Pinto, Diana C. G. A.,Silva, Artur M. S.

, p. 2683 - 2686 (2014/01/06)

An efficient one-pot synthesis of 3-methylflavone derivatives is established. Furthermore, their transformation into phosphorus ylides, which are then used in the diastereoselective synthesis of (E)-styrylflavones through Wittig reactions, is also studied

Lead optimization providing a series of flavone derivatives as potent nonsteroidal inhibitors of the cytochrome P450 aromatase enzyme

Gobbi, Silvia,Cavalli, Andrea,Rampa, Angela,Belluti, Federica,Piazzi, Lorna,Paluszcak, Anja,Hartmann, Rolf W.,Recanatini, Maurizio,Bisi, Alessandra

, p. 4777 - 4780 (2007/10/03)

Following our SAR studies on aromatase inhibitors, new compounds were designed by appropriately modifying the structure of flavone 1 using our previously reported CoMFA model. While the introduction of substituents on the 2-phenyl ring alone did not cause

Unsymmetrical Bichromonyl Benzene Derivatives from Formyl Flavones

Wurm, Gotthard,Nordmann, Matthias

, p. 555 - 558 (2007/10/02)

New flavones (4b-f/6) with formyl functions in the 3-, 4'-, 6- and 4',6-positions are synthesized from bromomethyl or dibromomethyl flavone derivatives (3a-e) with methylflavones (2a-e) as starting compounds.The formyl flavones are suitable synthetic tool

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