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2-Propen-1-one, 1-(3,5-dichloro-2-hydroxyphenyl)-3-(4-methoxyphenyl)-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62069-84-5

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62069-84-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62069-84-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,0,6 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 62069-84:
(7*6)+(6*2)+(5*0)+(4*6)+(3*9)+(2*8)+(1*4)=125
125 % 10 = 5
So 62069-84-5 is a valid CAS Registry Number.

62069-84-5SDS

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 3',5'-dichloro-2'-hydroxy-4-methoxy-trans-chalcone

1.2 Other means of identification

Product number -
Other names 3',5'-Dichlor-2'-hydroxy-4-methoxy-trans-chalkon

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:62069-84-5 SDS

62069-84-5Relevant academic research and scientific papers

Synthesis and biological activities of some flavones

Sawant,Gill,Nirwan

, p. 61 - 66 (2013/12/04)

Chalcones are synthesized by a base catalyzed Claisen Schmidt condensation reaction and then treated with dimethylsulphoxide in presence of iodine to get flavones. The synthesized compounds were evaluated for their antibacterial activity against Escherichia coilt P. aeruginosa, S. epidermidis and B. subtilis. All the flavones showed moderate to good activity. The structures of these compounds were confirmed by IR, UV, 1H NMR, Mass and elemental analysis.

CDK inhibitors having flavone structure

-

, (2008/06/13)

The present invention relates to a novel flavone derivative, pharmaceutically acceptable salt, hydrate, solvate and isomer thereof which is useful as an inhibitor against Cyclin Dependent Kinase (CDK), a process for preparation thereof, and a composition of anti-cancer agent or agent for treating neurodegenerative disease comprising this compound as an active ingredient.

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