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936924-39-9

C19H19NO2Te is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 936924-39-9 Structure

  • Basic information

    1. Product Name: C19H19NO2Te
    2. Synonyms: C19H19NO2Te
    3. CAS NO:936924-39-9
    4. Molecular Formula:
    5. Molecular Weight: 420.965
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 936924-39-9.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: C19H19NO2Te(CAS DataBase Reference)
    10. NIST Chemistry Reference: C19H19NO2Te(936924-39-9)
    11. EPA Substance Registry System: C19H19NO2Te(936924-39-9)

  • 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: 936924-39-9(Hazardous Substances Data)

936924-39-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 936924-39-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,6,9,2 and 4 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 936924-39:
(8*9)+(7*3)+(6*6)+(5*9)+(4*2)+(3*4)+(2*3)+(1*9)=209
209 % 10 = 9
So 936924-39-9 is a valid CAS Registry Number.

936924-39-9Downstream Products

936924-39-9Relevant articles and documents

Synthesis of isochalcogenazole rings by treating β-(N,N- dimethylcarbamoylchalcogenenyl)alkenyl ketones with hydroxylamine-O-sulfonic acid

Shimada, Kazuaki,Moro-oka, Akiko,Maruyama, Akiko,Fujisawa, Hiroyuki,Saito, Toshio,Kawamura, Ryo,Kogawa, Hisashi,Sakuraba, Maiko,Takata, Yukichi,Aoyagi, Shigenobu,Takikawa, Yuji,Kabuto, Chizuko

, p. 567 - 577 (2007)

β-(N,N-Dimethylcarbamoylselenenyl)- and β-(N,N- dimethylcarbamoyltellurenyl)alkenyl ketones were converted into isoselenazoles and isotellurazole Te-oxides, respectively, simply by treating with hydroxylamine-O-sulfonic acid, and deoxygenation of the latt

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