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CAS

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862422-06-8

3,3-dibenzyl-1-(toluene-4-sulfonyl)-pyrrolidin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 862422-06-8 Structure

  • Basic information

    1. Product Name: 3,3-dibenzyl-1-(toluene-4-sulfonyl)-pyrrolidin-2-one
    2. Synonyms: 3,3-dibenzyl-1-(toluene-4-sulfonyl)-pyrrolidin-2-one
    3. CAS NO:862422-06-8
    4. Molecular Formula:
    5. Molecular Weight: 419.544
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 862422-06-8.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: 3,3-dibenzyl-1-(toluene-4-sulfonyl)-pyrrolidin-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,3-dibenzyl-1-(toluene-4-sulfonyl)-pyrrolidin-2-one(862422-06-8)
    11. EPA Substance Registry System: 3,3-dibenzyl-1-(toluene-4-sulfonyl)-pyrrolidin-2-one(862422-06-8)

  • 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: 862422-06-8(Hazardous Substances Data)

862422-06-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 862422-06-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,2,4,2 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 862422-06:
(8*8)+(7*6)+(6*2)+(5*4)+(4*2)+(3*2)+(2*0)+(1*6)=158
158 % 10 = 8
So 862422-06-8 is a valid CAS Registry Number.

862422-06-8Relevant articles and documents

Synthesis of a novel series of 4,4-disubstituted 2,3,4,7-tetrahydroazepines

Barberis, Mario,García-Losada, Pablo,Pleite, Sehila,Rodríguez, Juan Ramón,Soriano, José Francisco,Mendiola, Javier

, p. 4847 - 4850 (2005)

A general, simple and straightforward strategy for the synthesis of a novel series of 4,4-disubstituted 2,3,4,7-tetrahydroazepines is described. This route involves a one-pot Wittig olefination/N-allylation process on a five-membered hemi-aminal followed by a final ring closing metathesis reaction.

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