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2-Butenoic acid, 4-[(4-aminophenyl)amino]-4-oxo-, (Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 71603-06-0 Structure
  • Basic information

    1. Product Name: 2-Butenoic acid, 4-[(4-aminophenyl)amino]-4-oxo-, (Z)-
    2. Synonyms:
    3. CAS NO:71603-06-0
    4. Molecular Formula: C10H10N2O3
    5. Molecular Weight: 206.201
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 71603-06-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-Butenoic acid, 4-[(4-aminophenyl)amino]-4-oxo-, (Z)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Butenoic acid, 4-[(4-aminophenyl)amino]-4-oxo-, (Z)-(71603-06-0)
    11. EPA Substance Registry System: 2-Butenoic acid, 4-[(4-aminophenyl)amino]-4-oxo-, (Z)-(71603-06-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 71603-06-0(Hazardous Substances Data)

71603-06-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71603-06-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,6,0 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 71603-06:
(7*7)+(6*1)+(5*6)+(4*0)+(3*3)+(2*0)+(1*6)=100
100 % 10 = 0
So 71603-06-0 is a valid CAS Registry Number.

71603-06-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (Z)-4-((4-aminophenyl)amino)-4-oxobut-2-enoic acid

1.2 Other means of identification

Product number -
Other names N-(4-aminophenyl)maleamic acid

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:71603-06-0 SDS

71603-06-0Relevant articles and documents

Synthesis and structural characterization of dendritic-linear PMA-APM-r-PS copolymers for a self-assembled microporous matrix

Hsieh, Shang-J.U.,Wang, Cheng-Chien,Chen, Chuh-Yung

, p. 3290 - 3301 (2010)

A set of dendritic-linear copolymers, poly(maleic anhydride-grafted-3, 3′-dimethyl-(4-aminophenylazanediyl)bis(2methylpropanoate)) -random-polystyrene (PMA-APM-r-PS), was successfully prepared by copolymerization of the novel dendritic macromonomer, 4-(4-

Isotope-Coded Maleimide Affinity Tags for Proteomics Applications

Wdowiak, Adam P.,Duong, Marisa N.,Joyce, Rohan D.,Boyatzis, Amber E.,Walkey, Mark C.,Nealon, Gareth L.,Arthur, Peter G.,Piggott, Matthew J.

, p. 1652 - 1666 (2021/07/20)

Isotope-coded affinity tags (ICATs) are valuable tools for mass spectrometry-based quantitative proteomics, in particular, for comparison of protein (cysteine-residue) thiol oxidation state in normal, stressed, and diseased tissue. However, the iodoacetam

RUBBER COMPOSITION

-

Paragraph 0185; 0186, (2015/09/28)

A rubber composition obtained by kneading at least one selected from the group consisting of (A1), (B1), (C1) and (D1), a rubber component and a filler, and a method of improving the viscoelastic property of vulcanized rubber, comprising a first step of kneading at least one selected from the group consisting of (A1), (B1), (C1) and (D1), a rubber component, a filler and a sulfur component and a second step of thermally treating the kneaded material obtained in the previous step. (A1): a compound represented by formula (I)(B1): a salt of a compound represented by formula (I)(C1): a solvate of a compound represented by formula (I)(D1): a solvate of a salt of a compound represented by formula (I)

Implantable material grafted with a cell antiproliferative and/or antibacterial film synthetized from a bifunctional molecule

-

Page/Page column, (2015/01/18)

The present invention relates to an implantable material having at least one external surface grafted with a film comprising carboxylate and sulfonate functions wherein the film is simultaneously synthesized and grafted directly on said external surface b

Binding of filamentous actin and winding into fibrillar aggregates by the polyphenolic C-glucosidic ellagitannin vescalagin

Quideau, Stephane,Douat-Casassus, Celine,Delannoy Lopez, Daniela Melanie,Di Primo, Carmelo,Chassaing, Stefan,Jacquet, Remi,Saltel, Frederic,Genot, Elisabeth

supporting information; experimental part, p. 5099 - 5104 (2011/06/26)

Winding it up: The plant polyphenolic metabolite vescalagin fulfills all the requirements for use as an antiactin agent in cellular biological investigations. Despite its high hydrophilicity, it rapidly enters cells and disturbs the organization of the actin cytoskeleton in a dose-dependent reversible manner by binding fibrillar actin and forcing the actin filaments (left) to wind themselves into ball-like fibrillar aggregates (right). Copyright

Solvent-free synthesis of arylamides and arylimides, analogues of acetylcholine

Trujillo-Ferrara,Correa-Basurto, Jose,Espinosa, Judith,Garcia, Jazmin,Martinez, Francisco,Miranda, Rene

, p. 2017 - 2023 (2007/10/03)

Several arylamides and arylimides, novel inhibitors of acetylcholinesterase, were obtained under solventless conditions; the target molecules were produced with a good overall yield and short reaction times. 2017-2023 Copyright Taylor & Francis, Inc.

The electronic effects on the formation of N-aryl-maleimides and isomaleimides

Fruk, Ljiljana,Graham, Duncan

, p. 2305 - 2313 (2007/10/03)

The synthesis of a range of aromatic maleimides and isomaleimides is reported. The effect of different substituents on the aromatic system and the products formed is also discussed.

INFLUENCE OF MEDIUM AND SUBSTITUENTS ON ACYLATION OF AROMATIC AMINES AND THEIR POLYMERIC ANALOGS WITH MALEIC ANHYDRIDE

Donya, A. P.,Pakter, M. K.,Sokhina, S. I.

, p. 2093 - 2097 (2007/10/02)

Correlation relationships describing the influence of substituents and solvents on the rate of acylation of aromatic amines and their polymeric analogs with maleic anhydride have been derived.

Functionalized Keggin- and Dawson-Type Cyclopentadienyltitanium Heteropolytungstate Anions: Small, Individually Distinguishable Labels for Conventional Transmission Elactron Microscopy. 2. Reactions

Keana, John F. W.,Ogan, Marc D.,Lue, YiXin,Beer, Michael,Varkey, J.

, p. 7957 - 7963 (2007/10/02)

Our goal is to develop a series of small, highly electron dense reagents to label substrate molecules covalently and chemoselectively for subsequent visualisation by using conventional transmission electron microscopy (CTEM).Starting with the organic functionalized cyclopentadienyltitanium (CpTi) substituted Keggin- and Dawson-type heteropolytungstate (HPT) anions prepared in the accompanying paper, it was first established that the HPT unit as well as the Cp-Ti bond in those anions are stable under a variety of reaction conditions that lead to modification (esterification, acylation, reduction, reductive amination, oxidation, and cycloaddition reactions) of the organic appendage.A Diels-Alder reaction between either Keggin HPT diene 34 or Dawson HPT diene 18 and one of several substituted N-phenylmaleimides (27-33) was a versatile method for the attachment of a variety of protein-reactive groups to the HPT anions.Thus prepared were HPT maleimides 20 and 35, bromoacetamides 21 and 36, biotin derivative 22, isothiocyanate 24, and N-hydroxysuccinimide esters 37 and 40.Additionally, the new heterobifunctional dienophiles 29, 30, 32 and 33 should act as protein cross-linking agents, complementing those already available.Acylating agent 40 is noteworthy in that two Dawson HPT units are tethered in close proximity to each other in this reagent.By analogy to the EM image of "dimeric" HPT 23, the EM image of 40 is expected to be recognizable morphologically as dumbells.HPT-labeled ATP derivative 42 was prepared by a reductive amination of Dawson benzaldehyde 10 with N6-methyl>ATP (Li salt).Both Keggin and Dawson HPTs are visible individually by using CTEM.Their stability in the electron beam is high.

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