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Propanoic acid, 3-oxo-3-[(3,4,5-trimethoxyphenyl)amino]-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65051-18-5

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65051-18-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65051-18-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,0,5 and 1 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 65051-18:
(7*6)+(6*5)+(5*0)+(4*5)+(3*1)+(2*1)+(1*8)=105
105 % 10 = 5
So 65051-18-5 is a valid CAS Registry Number.

65051-18-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 3-oxo-3-(3,4,5-trimethoxyphenylamino)propanoate

1.2 Other means of identification

Product number -
Other names 3.4.5-Trimethoxyphenylcarbamoylessigsaeureethylester

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:65051-18-5 SDS

65051-18-5Relevant academic research and scientific papers

Design and synthesis of novel substituted indole-acrylamide derivatives and evaluation of their anti-cancer activity as potential tubulin-targeting agents

Baytas, Sultan Nacak,Cetin-Atalay, Rengul,Ergun, Sezen Guntekin,Hamel, Ernest,Hawash, Mohammed,Kahraman, Deniz Cansen,Olgac, Abdurrahman

, (2022/01/19)

Novel compounds containing polar and nonpolar substitutions on the prop-2-en-1-on linker of the trans-indol-3-ylacrylamide scaffold were designed by modeling within the colchicine site of tubulin and then synthesized to determine the role of such substitu

Malonic ester amide synthesis: An efficient methodology for synthesis of amides

Mahajan, Pankaj S.,Mahajan, Jyoti P.,Mhaske, Santosh B.

, p. 2508 - 2516 (2013/07/25)

A general methodology malonic ester amide synthesis has been demonstrated, which uses α-substituted/unsubstituted diethyl malonates for the decarboxylative acylation of various aromatic/heteroaromatic primary/secondary amines to form one-carbon homologated amides, thus providing easy access to amides with odd/even chain lengths and an array of substituents on the alkyl/aryl part while avoiding use of acyl chlorides or peptide coupling reagents. Copyright

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