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299209-91-9

(R)-(+)-(3,4-dimethoxybenzylidene)-p-toluenesulfinamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 299209-91-9 Structure

  • Basic information

    1. Product Name: (R)-(+)-(3,4-dimethoxybenzylidene)-p-toluenesulfinamide
    2. Synonyms: (R)-(+)-(3,4-dimethoxybenzylidene)-p-toluenesulfinamide
    3. CAS NO:299209-91-9
    4. Molecular Formula:
    5. Molecular Weight: 303.382
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 299209-91-9.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: (R)-(+)-(3,4-dimethoxybenzylidene)-p-toluenesulfinamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-(+)-(3,4-dimethoxybenzylidene)-p-toluenesulfinamide(299209-91-9)
    11. EPA Substance Registry System: (R)-(+)-(3,4-dimethoxybenzylidene)-p-toluenesulfinamide(299209-91-9)

  • 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: 299209-91-9(Hazardous Substances Data)

299209-91-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 299209-91-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,9,2,0 and 9 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 299209-91:
(8*2)+(7*9)+(6*9)+(5*2)+(4*0)+(3*9)+(2*9)+(1*1)=189
189 % 10 = 9
So 299209-91-9 is a valid CAS Registry Number.

299209-91-9Relevant articles and documents

Alkaloid synthesis using chiral δ-amino β-ketoesters: A stereoselective synthesis of (-)-lasubine II

Davis, Franklin A.,Chao, Bin

, p. 2623 - 2625 (2000)

(equation presented) A highly stereoselective asymmetric synthesis of the quinolizidine alkaloid (-)-lasubine II from a δ-amino β-hydroxy ketone, a new polyfunctionalized chiral building block, is described.

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