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CAS

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101289-00-3

N'-allyl-N'-phenyltosylhydrazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 101289-00-3 Structure

  • Basic information

    1. Product Name: N'-allyl-N'-phenyltosylhydrazide
    2. Synonyms: N'-allyl-N'-phenyltosylhydrazide
    3. CAS NO:101289-00-3
    4. Molecular Formula:
    5. Molecular Weight: 302.397
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 101289-00-3.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'-allyl-N'-phenyltosylhydrazide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N'-allyl-N'-phenyltosylhydrazide(101289-00-3)
    11. EPA Substance Registry System: N'-allyl-N'-phenyltosylhydrazide(101289-00-3)

  • 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: 101289-00-3(Hazardous Substances Data)

101289-00-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 101289-00-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,2,8 and 9 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 101289-00:
(8*1)+(7*0)+(6*1)+(5*2)+(4*8)+(3*9)+(2*0)+(1*0)=83
83 % 10 = 3
So 101289-00-3 is a valid CAS Registry Number.

101289-00-3Downstream Products

101289-00-3Relevant articles and documents

Rhodium(II)-Catalyzed Synthesis of N-Aryl-N′-tosyldiazenes from Primary Aromatic Amines Using (Tosylimino)aryliodinane: A Potent Stable Surrogate for Diazonium Salts

Ito, Motoki,Tanaka, Arisa,Higuchi, Kazuhiro,Sugiyama, Shigeo

, p. 1272 - 1276 (2017)

A single-step synthesis of N-aryl-N′-tosyldiazenes from primary aromatic amines was developed. A wide range of aromatic amines provided the corresponding products in high yields by N–N bond formation with RhII–nitrene intermediates, which were generated in situ from dirhodium(II) complex catalysts and (tosylimino)-2,4,6-trimethylphenyliodinane, followed by oxidation. The synthesized N-aryl-N′-tosyldiazenes were successfully demonstrated to serve as potent and stable surrogates for diazonium salts in the two-step deaminative transformation of primary aromatic amines.

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