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113985-17-4

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113985-17-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 113985-17-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,9,8 and 5 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 113985-17:
(8*1)+(7*1)+(6*3)+(5*9)+(4*8)+(3*5)+(2*1)+(1*7)=134
134 % 10 = 4
So 113985-17-4 is a valid CAS Registry Number.

113985-17-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(pyridyl-2 methyl)(hydroxy-4 methoxy-3 phenyl)-3 propene-2 amide

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:113985-17-4 SDS

113985-17-4Downstream Products

113985-17-4Relevant articles and documents

Ferulic acid amide derivatives as anticancer and antioxidant agents: synthesis, thermal, biological and computational studies

Kumar, Naresh,Kumar, Sandeep,Abbat, Sheenu,Nikhil, Kumar,Sondhi, Sham M.,Bharatam, Prasad V.,Roy, Partha,Pruthi, Vikas

, p. 1175 - 1192 (2016/07/06)

Abstract: The design and microwave-assisted synthesis of four series (IIIa–IIIo, Va–Vg, VIIa–VIIg and IXa–IXe) of mono and bis-amide derivatives of ferulic acid have been achieved under solvent-free conditions and, subsequently characterized by spectroscopic techniques. During thermal analysis, all the compounds were found stable up to 100?°C and decomposed through single step at higher temperature. The derivatives were screened for their in vitro cytotoxicity and antioxidant activity, respectively and observed that compound Vb was most active against breast (MCF-7; IC50?=?07.49?μM and MDA-MB-231; IC50?=?07.28?μM), Vd against lung (A549; IC50?=?07.11?μM) and liver (HepG2; IC50?=?08.32?μM), and Ve against cervical (HeLa; IC50?=?07.14?μM) cancer cell lines, while compounds IIIf, IIIl, IIIo, VIIe and IXa–IXe were found to exhibit the strong antioxidant activity with respect to their parent molecule. Previous reports for the biological applications of ferulic acid amides also confirmed the importance of work presented here. The 3D-QSAR studies for anticancer and antioxidant activities were also performed by using CoMFA, and the corresponding contour maps of electrostatic and steric fields have been computed. Statistical analysis between experimental and CoMFA-predicted data for pIC50 have been accomplished by curve fitting analysis which showed the significant correlation. Graphical Abstract: [Figure not available: see fulltext.]

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