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1450735-40-6

N-[3-butyl-4-tosylazet-2(1H)-ylidene]methanesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1450735-40-6 Structure

  • Basic information

    1. Product Name: N-[3-butyl-4-tosylazet-2(1H)-ylidene]methanesulfonamide
    2. Synonyms:
    3. CAS NO:1450735-40-6
    4. Molecular Formula:
    5. Molecular Weight: 356.467
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1450735-40-6.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-[3-butyl-4-tosylazet-2(1H)-ylidene]methanesulfonamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-[3-butyl-4-tosylazet-2(1H)-ylidene]methanesulfonamide(1450735-40-6)
    11. EPA Substance Registry System: N-[3-butyl-4-tosylazet-2(1H)-ylidene]methanesulfonamide(1450735-40-6)

  • 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: 1450735-40-6(Hazardous Substances Data)

1450735-40-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1450735-40-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,0,7,3 and 5 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1450735-40:
(9*1)+(8*4)+(7*5)+(6*0)+(5*7)+(4*3)+(3*5)+(2*4)+(1*0)=146
146 % 10 = 6
So 1450735-40-6 is a valid CAS Registry Number.

1450735-40-6Downstream Products

1450735-40-6Relevant articles and documents

Synthesis of functionalized azet-2(1 H)-imines through [2+2] cycloaddition of imines and ketenimines

Yavari, Issa,Nematpour, Manijeh

, p. 1420 - 1422 (2013)

The reaction between ketenimine intermediates, generated from terminal alkynes and sulfonyl azides, trichloroacetonitrile, and sodium arylsulfinates in N,N-dimethylformamide at room temperature affords N-[3-aryl(alkyl)-4-arylazet- 2(1H)-ylidene]-arene(alk

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