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CAS

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144782-49-0

Benzyl-[1-phenyl-2-((R)-toluene-4-sulfinyl)-eth-(E)-ylidene]-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 144782-49-0 Structure

  • Basic information

    1. Product Name: Benzyl-[1-phenyl-2-((R)-toluene-4-sulfinyl)-eth-(E)-ylidene]-amine
    2. Synonyms: Benzyl-[1-phenyl-2-((R)-toluene-4-sulfinyl)-eth-(E)-ylidene]-amine
    3. CAS NO:144782-49-0
    4. Molecular Formula:
    5. Molecular Weight: 347.481
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 144782-49-0.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: Benzyl-[1-phenyl-2-((R)-toluene-4-sulfinyl)-eth-(E)-ylidene]-amine(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzyl-[1-phenyl-2-((R)-toluene-4-sulfinyl)-eth-(E)-ylidene]-amine(144782-49-0)
    11. EPA Substance Registry System: Benzyl-[1-phenyl-2-((R)-toluene-4-sulfinyl)-eth-(E)-ylidene]-amine(144782-49-0)

  • 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: 144782-49-0(Hazardous Substances Data)

144782-49-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144782-49-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,7,8 and 2 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 144782-49:
(8*1)+(7*4)+(6*4)+(5*7)+(4*8)+(3*2)+(2*4)+(1*9)=150
150 % 10 = 0
So 144782-49-0 is a valid CAS Registry Number.

144782-49-0Relevant articles and documents

Synthesis and stereoselective reductions of chiral β-iminosulfoxides

Garcia Ruano,Lorente,Rodriguez

, p. 5637 - 5640 (1992)

Reaction of chiral non racemic β-ketosulfoxides with amines or condensation of the imine enolates with (-)-menthyl sulfinate yield optically pure β-iminosulfoxides. The second method requires the presence of an excess of MgBr2 in order to avoid

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