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2-Propen-1-one, 3-[5-(4-bromophenyl)-2-furanyl]-1-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

20005-40-7

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20005-40-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20005-40-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,0,0 and 5 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 20005-40:
(7*2)+(6*0)+(5*0)+(4*0)+(3*5)+(2*4)+(1*0)=37
37 % 10 = 7
So 20005-40-7 is a valid CAS Registry Number.

20005-40-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Propen-1-one, 3-[5-(4-bromophenyl)-2-furanyl]-1-phenyl- (en)

1.2 Other means of identification

Product number -
Other names -

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:20005-40-7 SDS

20005-40-7Relevant academic research and scientific papers

Synthesis of novel arylfurfurylchalcones

Aslam, Samina,Asif, Nadia,Khan, Muhammad Naeem,Khan, Misbahul Ain,Munawar, Munawar Ali,Nasrullah, Muhammad

, p. 7738 - 7742 (2013/09/23)

Various aryl furans-2-carbaldehyde chalcones with different acetophenones were prepared and characterized through their elemental analyses and spectroscopic techniques (FTIR, 1H NMR, 13C NMR and mass spectra).

Studies on arylfuran derivatives Part X. Synthesis and antibacterial properties of arylfuryl-Δ2-pyrazolines

Shivarama Holla,Akberali,Shivananda

, p. 256 - 263 (2007/10/03)

Arylfurylpropenones 3 were synthesized by Claisen-Schmidt condensation of arylfurfurals 1 with various substituted acetophenones 2. Cyclocondensation of these arylfurylpropenones 3 with hydrazine hydrate and phenylhydrazine furnished 1H-pyrazolines 4 and N-phenylpyrazolines 6, respectively. In order to study the structure-activity relationships, pyrazolines 4 were converted into their N-acetyl derivatives 5. The antibacterial properties of the new pyrazoline derivatives were studied. (C) 2000 Elsevier Science S.A.

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