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

112753-54-5

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112753-54-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112753-54-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,7,5 and 3 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 112753-54:
(8*1)+(7*1)+(6*2)+(5*7)+(4*5)+(3*3)+(2*5)+(1*4)=105
105 % 10 = 5
So 112753-54-5 is a valid CAS Registry Number.

112753-54-5SDS

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-(4-methoxyphenyl)-1-(5-methylfuran-2-yl)prop-2-en-1-one

1.2 Other means of identification

Product number -
Other names 1-(5-methylfuryl-2)-3-(4'-methoxyphenyl)propenone-2

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:112753-54-5 SDS

112753-54-5Relevant academic research and scientific papers

Compound capable of effectively inhibiting or killing multi-drug resistant bacteria and preparation method and application of compound

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Paragraph 0185; 0708, (2017/06/02)

The invention discloses a compound capable of effectively inhibiting or killing bacterial microorganisms. The compound has a structural general formula shown as the formula I (please see the formula in the description). Pharmacodynamic experiments prove that the compound can effectively inhibit or kill the broad-spectrum and multi-drug resistant staphylococcus aureus, streptococcus pneumoniae and staphylococcus aureus and is expected to be developed into a novel effective antibacterial drug with new targets.

Design, synthesis, and anti-influenza viral activities of 1,3-diarylprop-2-en-1-ones: A novel class of neuraminidase inhibitors

Kinger, Mayank,Park, Yong Dae,Park, Jeong Hoon,Hur, Min Goo,Jeong, Hyung Jae,Park, Su-Jin,Lee, Woo Song,Kim, Sang Wook,Yang, Seung Dae

experimental part, p. 633 - 638 (2012/09/21)

A series of 1,3-diarylprop-2-en-1-one derivatives 3a-v have been synthesized and evaluated for their ability to inhibit neuraminidase (NA). Among the prepared compounds, the less lipophilic derivative 3k showed the most potent in vitro inhibitory activity against NA with an IC50 value of 1.5 μM.

Synthesis and In Vitro Antifungal Evaluation of 1,3,5-Trisubstituted-2-Pyrazoline Derivatives

Deng, Hui,Yu, Zhi-Yi,Shi, Guan-Ying,Chen, Ming-Jing,Tao, Ke,Hou, Tai-Ping

experimental part, p. 279 - 289 (2012/05/20)

Pyrazolines, the well-known five-membered nitrogen-containing heterocyclic compounds, have received considerable interests in the fields of medicinal and agricultural chemistry because of their broad spectrum of biological activities. To discover more pot

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