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1230-77-9

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1230-77-9 Usage

Backbone Structure

1-(4-methoxyphenyl)prop-2-en-1-one

Functional Groups

4-(dimethylamino)phenyl group
Structure: -N(CH3)2 attached at the third position
Functional Significance: Common in drugs and biologically active molecules, suggests potential pharmacological or biological activity
4-methoxyphenyl group
Structure: -OCH3 attached
Functional Significance: Modulates properties of compounds it's attached to, may contribute to biological or pharmacological activity

Biological/Pharmacological Activity

Likely to exhibit some level of activity in these areas due to the presence of functional groups commonly associated with such activity.

Potential for Investigation

Could be of interest for further research and investigation in biological and pharmacological contexts.

Check Digit Verification of cas no

The CAS Registry Mumber 1230-77-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,3 and 0 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1230-77:
(6*1)+(5*2)+(4*3)+(3*0)+(2*7)+(1*7)=49
49 % 10 = 9
So 1230-77-9 is a valid CAS Registry Number.

1230-77-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-3-(4-(dimethylamino)phenyl)-1-(4-methoxyphenyl)prop-2-en-1-one

1.2 Other means of identification

Product number -
Other names 4-Dimethylamino-4'-methoxy-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:1230-77-9 SDS

1230-77-9Relevant articles and documents

Electrosynthesis and characterization of a new semi-conducting oligomer deriving from a disubstituted chalcone: 4-dimethylamino -4′-methoxychalcone

Messaoudi, Ilhem,Aribi, Imen,Zaaboub, Zouhour,Ayachi, Sahbi,Othman, Mohamed,Said, Ayoub Haj

, (2021)

An oligo phenylene vinylene was electrosynthesized by the anodic oxidation of the 4-dimethylamino-4′-methoxychalcone (DMAMC) at a constant potential in nitromethane on a platinum electrode. 1H and 13C NMR, FTIR and UV spectroscopy, c

Pyrazoline analogs as potential anticancer agents and their apoptosis, molecular docking, MD simulation, DNA binding and antioxidant studies

Rana, Manish,Arif, Rizwan,Khan, Faez Iqbal,Maurya, Vikas,Singh, Raja,Faizan, Md Imam,Yasmeen, Shama,Dar, Sajad Hussain,Alam, Raquib,Sahu, Ankita,Ahmad, Tanveer,Rahisuddin

, (2021/02/12)

N-formyl pyrazoline derivatives (3a–3l) were designed and synthesized via Michael addition reaction through cyclization of chalcones with hydrazine hydrate in presence of formic acid. The structural elucidation of N-formyl pyrazoline derivatives was carri

Photodynamic treatment of melanoma cells using aza-dipyrromethenes as photosensitizers

Biazzotto, Juliana C.,Castro, Kelly A. D. F.,Costa, Letícia D.,Da Silva, Roberto S.,Faustino, M. Amparo F.,Guieu, Samuel,Neves, Maria Da Gra?a P. M. S.,Tomé, Augusto C.

, p. 885 - 891 (2020/07/23)

In this study, we report for the first time the use of four aza-dipyrromethenes (ADPMs) as photosensitizers for cancer PDT. The synthesis and characterization of the ADPMs and their photodynamic action against B16F10 melanoma cells were assessed. ADPM 2 i

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