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1226859-16-0

C29H32N6O3S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1226859-16-0 Structure

  • Basic information

    1. Product Name: C29H32N6O3S
    2. Synonyms:
    3. CAS NO:1226859-16-0
    4. Molecular Formula:
    5. Molecular Weight: 544.677
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1226859-16-0.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: C29H32N6O3S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C29H32N6O3S(1226859-16-0)
    11. EPA Substance Registry System: C29H32N6O3S(1226859-16-0)

  • 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: 1226859-16-0(Hazardous Substances Data)

1226859-16-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1226859-16-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,6,8,5 and 9 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1226859-16:
(9*1)+(8*2)+(7*2)+(6*6)+(5*8)+(4*5)+(3*9)+(2*1)+(1*6)=170
170 % 10 = 0
So 1226859-16-0 is a valid CAS Registry Number.

1226859-16-0Downstream Products

1226859-16-0Relevant articles and documents

Azodicarhoxamides vs. azodicarboxylates in reactions against thioisomuenchnones: 1,3-dipolar cycloaddition or nucleophilic addition?

Sanchez, Barbara,Lopez, Ignacio,Light, Mark E.,Silvero, Guadalupe,Bravo, Jose Luis

, p. 1648 - 1652 (2010)

This communication presents the first study on the use of azodicarboxamides against mesoionic heterocycles as 1,3-dipoles. The reactions yield thioureido compounds. Their formation could be explained, on the basis of experimental results and preliminary theoretical calculations, by a nucleophilic addition followed by rearrangement; however, a formal 1,3-dipolar cycloaddition and subsequent fragmentation and rearrangement of the transient cycloadducts could not be ruled out. Reactions are carried out in refluxing toluene and are complete in 90-240 min. Structural elucidation of the products is based on single-crystal X-ray analysis, as well as other spectroscopic data and 2D-NMR correlations.

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