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1001067-54-4

N-ethyl-N-(2-(prop-2-yn-1-yloxy)ethyl)aniline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1001067-54-4 Structure

  • Basic information

    1. Product Name: N-ethyl-N-(2-(prop-2-yn-1-yloxy)ethyl)aniline
    2. Synonyms: N-ethyl-N-(2-(prop-2-yn-1-yloxy)ethyl)aniline
    3. CAS NO:1001067-54-4
    4. Molecular Formula:
    5. Molecular Weight: 203.284
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1001067-54-4.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: N-ethyl-N-(2-(prop-2-yn-1-yloxy)ethyl)aniline(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-ethyl-N-(2-(prop-2-yn-1-yloxy)ethyl)aniline(1001067-54-4)
    11. EPA Substance Registry System: N-ethyl-N-(2-(prop-2-yn-1-yloxy)ethyl)aniline(1001067-54-4)

  • 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: 1001067-54-4(Hazardous Substances Data)

1001067-54-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1001067-54-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,1,0,6 and 7 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1001067-54:
(9*1)+(8*0)+(7*0)+(6*1)+(5*0)+(4*6)+(3*7)+(2*5)+(1*4)=74
74 % 10 = 4
So 1001067-54-4 is a valid CAS Registry Number.

1001067-54-4Relevant articles and documents

Self-assembly of fluorescent inclusion complexes in competitive media including the interior of living cells

Gassensmith, Jeremiah J.,Arunkumar, Easwaran,Barr, Lorna,Baumes, Jeffrey M.,DiVittorio, Kristy M.,Johnson, James R.,Noll, Bruce C.,Smith, Bradley D.

, p. 15054 - 15059 (2007)

Anthracene-containing tetralactam macrocycles are prepared and found to have an extremely high affinity for squaraine dyes in chloroform (log K a = 5.2). Simply mixing the two components produces highly fluorescent, near-infrared inclusion comp

High-Frequency Mechanostimulation of Cell Adhesion

Kadem, Laith F.,Suana, K. Grace,Holz, Michelle,Wang, Wei,Westerhaus, Hannes,Herges, Rainer,Selhuber-Unkel, Christine

, p. 225 - 229 (2017)

Cell adhesion is regulated by molecularly defined protein interactions and by mechanical forces, which can activate a dynamic restructuring of adhesion sites. Previous attempts to explore the response of cell adhesion to forces have been limited to applying mechanical stimuli that involve the cytoskeleton. In contrast, we here apply a new, oscillatory type of stimulus through push–pull azobenzenes. Push–pull azobenzenes perform a high-frequency, molecular oscillation upon irradiation with visible light that has frequently been applied in polymer surface relief grating. We here use these oscillations to address single adhesion receptors. The effect of molecular oscillatory forces on cell adhesion has been analyzed using single-cell force spectroscopy and gene expression studies. Our experiments demonstrate a reinforcement of cell adhesion as well as upregulated expression levels of adhesion-associated genes as a result of the nanoscale “tickling” of integrins. This novel type of mechanical stimulus provides a previously unprecedented molecular control of cellular mechanosensing.

Red emitting neutral fluorescent glycoconjugates for membrane optical imaging

Redon, Sébastien,Massin, Julien,Pouvreau, Sandrine,De Meulenaere, Evelien,Clays, Koen,Queneau, Yves,Andraud, Chantal,Girard-Egrot, Agnés,Bretonniére, Yann,Chambert, Stéphane

, p. 773 - 787 (2014/05/06)

A family of neutral fluorescent probes was developed, mimicking the overall structure of natural glycolipids in order to optimize their membrane affinity. Nonreducing commercially available di- or trisaccharidic structures were connected to a push-pull ch

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