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541520-03-0

N-phenyl-4-isopropylcinnamamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 541520-03-0 Structure

  • Basic information

    1. Product Name: N-phenyl-4-isopropylcinnamamide
    2. Synonyms: N-phenyl-4-isopropylcinnamamide
    3. CAS NO:541520-03-0
    4. Molecular Formula:
    5. Molecular Weight: 265.355
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 541520-03-0.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: N-phenyl-4-isopropylcinnamamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-phenyl-4-isopropylcinnamamide(541520-03-0)
    11. EPA Substance Registry System: N-phenyl-4-isopropylcinnamamide(541520-03-0)

  • 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: 541520-03-0(Hazardous Substances Data)

541520-03-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 541520-03-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,4,1,5,2 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 541520-03:
(8*5)+(7*4)+(6*1)+(5*5)+(4*2)+(3*0)+(2*0)+(1*3)=110
110 % 10 = 0
So 541520-03-0 is a valid CAS Registry Number.

541520-03-0Relevant articles and documents

Oxindole synthesis by palladium-catalysed aromatic C-H alkenylation

Ueda, Satoshi,Okada, Takahiro,Nagasawa, Hideko

, p. 2462 - 2464 (2010)

A strategy involving palladium-catalysed aromatic C-H functionalisation/ intramolecular alkenylation provides a convenient and direct synthesis of 3-alkylideneoxindoles. In the presence of 5 mol% of PdCl2MeCN 2 and AgOCOCF3, a wide variety of N-cinnamoylanilines gave 3-alkylideneoxindoles in moderate to good yield. The Royal Society of Chemistry.

Cinnamides as selective small-molecule inhibitors of a cellular model of breast cancer stem cells

Germain, Andrew R.,Carmody, Leigh C.,Nag, Partha P.,Morgan, Barbara,Verplank, Lynn,Fernandez, Cristina,Donckele, Etienne,Feng, Yuxiong,Perez, Jose R.,Dandapani, Sivaraman,Palmer, Michelle,Lander, Eric S.,Gupta, Piyush B.,Schreiber, Stuart L.,Munoz, Benito

supporting information, p. 1834 - 1838 (2013/04/10)

A high-throughput screen (HTS) was conducted against stably propagated cancer stem cell (CSC)-enriched populations using a library of 300,718 compounds from the National Institutes of Health (NIH) Molecular Libraries Small Molecule Repository (MLSMR). A cinnamide analog displayed greater than 20-fold selective inhibition of the breast CSC-like cell line (HMLE-sh-Ecad) over the isogenic control cell line (HMLE-sh-eGFP). Herein, we report structure-activity relationships of this class of cinnamides for selective lethality towards CSC-enriched populations.

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