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1201667-71-1

C54H56O4 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1201667-71-1 Structure

  • Basic information

    1. Product Name: C54H56O4
    2. Synonyms:
    3. CAS NO:1201667-71-1
    4. Molecular Formula:
    5. Molecular Weight: 769.036
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1201667-71-1.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: C54H56O4(CAS DataBase Reference)
    10. NIST Chemistry Reference: C54H56O4(1201667-71-1)
    11. EPA Substance Registry System: C54H56O4(1201667-71-1)

  • 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: 1201667-71-1(Hazardous Substances Data)

1201667-71-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1201667-71-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,1,6,6 and 7 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1201667-71:
(9*1)+(8*2)+(7*0)+(6*1)+(5*6)+(4*6)+(3*7)+(2*7)+(1*1)=121
121 % 10 = 1
So 1201667-71-1 is a valid CAS Registry Number.

1201667-71-1Upstream product

1201667-71-1Downstream Products

1201667-71-1Relevant articles and documents

Axially chiral facial amphiphiles with a dihydronaphthopentaphene structure as molecular tweezers for swnts

Marquis, Renaud,Kulikiewicz, Krystyna,Lebedkin, Sergei,Kappes, Manfred M.,Meunier, Charles Mioskowski Stephane,Wagner, Alain

, p. 11187 - 11196 (2009)

Syntheses of chiral 6,15dihydronaphtho[2,3-c]pentaphene derivatives of opposite configurations are reported. Starting from anthracene, the strategy involves two key steps: a Diels-Alder reaction on a prochiral dianthraquinone, and an enantiomeric resolution using (-)-menthol. The final molecules exhibit very strong optical activity, as shown by their circular dichroism spectra, and are examples of chiral facial amphiphiles. Their adsorption at the surface of single-walled carbon nanotubes (SWNTs) has also been studied, and has been found to occur preferentially on 0.8-1.0 nm diameter nanotubes among the population of a high-pressure CO conversion (HiPco) SWNT sample (0.8-1.2 nm). The synthesised facial amphiphiles act as nano-tweezers for the diameter-selective solubilisation of SWNTs in water. The expected optical activities of the SWNT samples solubilised by each of the chiral amphiphiles have been studied by circular dichroism spectroscopy, but the results are not yet conclusive.

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