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2-Butenedioic acid, 2-[(2-nitrophenyl)amino]-, dimethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17454-33-0

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17454-33-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17454-33-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,4,5 and 4 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 17454-33:
(7*1)+(6*7)+(5*4)+(4*5)+(3*4)+(2*3)+(1*3)=110
110 % 10 = 0
So 17454-33-0 is a valid CAS Registry Number.

17454-33-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl 2-(2-nitroanilino)but-2-enedioate

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:17454-33-0 SDS

17454-33-0Relevant academic research and scientific papers

Assembly and optical properties of 1D helical bundles induced by triphenylamine, side chains and solvents in crystals

Li, Baolin,Pang, Zhi,Qi, Ting

supporting information, p. 5555 - 5562 (2021/07/02)

Two novel helical aromatic foldamer derivativesTPA-Q6(n-He)andTPA-Q6(i-Bu)were synthesized and characterized by introducingn-hexyloxy and isobutoxy side chains, respectively, and modifying quinoline amide foldamers with the triphenyl

Foldamer-Based Potassium Channels with High Ion Selectivity and Transport Activity

Qi, Shuaiwei,Zhang, Chenyang,Yu, Hao,Zhang, Jing,Yan, Tengfei,Lin, Ze,Yang, Bing,Dong, Zeyuan

supporting information, p. 3284 - 3288 (2021/04/07)

Small molecules that independently perform natural channel-like functions show greatly potential in the treatment of human diseases. Taking advantage of aromatic helical scaffolds, we develop a kind of foldamer-based ion channels with lumen size varying f

Folding of a linear array of α-amino acids within a helical aromatic oligoamide frame

Kudo, Mayumi,Maurizot, Victor,Kauffmann, Brice,Tanatani, Aya,Huc, Ivan

supporting information, p. 9628 - 9631 (2013/07/26)

Control of the spatial organization of proteinogenic side chains is critical for the development of protein mimics with selective recognition properties toward target protein surfaces. We present a novel methodology for producing a linear array of protein

Synthesis of bisquinoline-pyrrole oligoamide as G-quadruplex binding ligand

Ong, Chi Wi,Liu, Meng-Chi,Lee, Kun-Da,Chang, Keng Wei,Yang, Ya-Ting,Tung, Hung-Wei,Fox, Keith R.

scheme or table, p. 5453 - 5457 (2012/09/08)

A one-pot procedure using ammonium formate under palladium catalysis for the reductive dechlorination and reduction of nitro group of 4-chloro-8-nitro-quinoline derivatives has be successfully carried out. This has lead to the synthesis of bisquinoline-py

Compositions derived from quinoline and quinoxaline, preparation and use thereof

-

Page/Page column 24, (2008/06/13)

The present invention concerns compounds derived from quinoline and quinoxaline, their preparation and their uses, particularly in the field of therapeutics and vaccines or for developing active compounds. The inventive compounds are of general formula (I

Synthesis and antiallergic activity of some quinolinones and imidazoquinolinones

Peet,Baugh,Sunder,Lewis

, p. 298 - 302 (2007/10/02)

A group of 1,4-dihydro-4-oxoquinoline-2- and 3-carboxylic acid esters with nitrogen functionality at the 8-position was synthesized, and 6-oxo-6H-imidazo[4,5,1-ij]quinoline-4- and 5-carboxylic acid esters were elaborated from these. Several of the compoun

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