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1418317-72-2

C33H35NO2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1418317-72-2 Structure

  • Basic information

    1. Product Name: C33H35NO2
    2. Synonyms: C33H35NO2
    3. CAS NO:1418317-72-2
    4. Molecular Formula:
    5. Molecular Weight: 477.646
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1418317-72-2.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: C33H35NO2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C33H35NO2(1418317-72-2)
    11. EPA Substance Registry System: C33H35NO2(1418317-72-2)

  • 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: 1418317-72-2(Hazardous Substances Data)

1418317-72-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1418317-72-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,8,3,1 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1418317-72:
(9*1)+(8*4)+(7*1)+(6*8)+(5*3)+(4*1)+(3*7)+(2*7)+(1*2)=152
152 % 10 = 2
So 1418317-72-2 is a valid CAS Registry Number.

1418317-72-2Downstream Products

1418317-72-2Relevant articles and documents

A screw-shaped alignment of pyrene using m-calix[3]amide

Yamakado, Ryohei,Matsuoka, Shin-Ichi,Suzuki, Masato,Takagi, Koji,Katagiri, Kosuke,Azumaya, Isao

, p. 1516 - 1520 (2013)

m-Calix[3]amide bearing three pyrenes (1a) was prepared by the condensation reaction of 3-nonylaminobenzoic acid derivative using Ph3PCl 2. Pyrenyl groups were found to be aligned in the screw-like fashion by m-calix[3]amide as confirmed by the X-ray crystallography. Aromatic proton signals observed at the up-field region in the 1H NMR spectrum at low temperature indicated that pyrenyl groups in 1a are aligned in close proximity in THF solution. UV-vis absorption and fluorescence emission spectra did not show marked peak shift nor concentration fluorescence quenching compared with reference compounds implying no significant electronic interaction between pyrenyl groups. These results can be explained by the steric effect of the m-calix[3]amide platform. On the other hand, an excimer emission was observed for m-calix[3]amide having a flexible spacer between pyrene and m-calix[3]amide (1b).

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