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945026-41-5

2-[Methyl-(4-Methyl-benzyl)-aMino]-ethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 945026-41-5 Structure

  • Basic information

    1. Product Name: 2-[Methyl-(4-Methyl-benzyl)-aMino]-ethanol
    2. Synonyms: 2-[Methyl-(4-Methyl-benzyl)-aMino]-ethanol
    3. CAS NO:945026-41-5
    4. Molecular Formula: C11H17NO
    5. Molecular Weight: 179.25878
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 945026-41-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-[Methyl-(4-Methyl-benzyl)-aMino]-ethanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-[Methyl-(4-Methyl-benzyl)-aMino]-ethanol(945026-41-5)
    11. EPA Substance Registry System: 2-[Methyl-(4-Methyl-benzyl)-aMino]-ethanol(945026-41-5)

  • 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: 945026-41-5(Hazardous Substances Data)

945026-41-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 945026-41-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,5,0,2 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 945026-41:
(8*9)+(7*4)+(6*5)+(5*0)+(4*2)+(3*6)+(2*4)+(1*1)=165
165 % 10 = 5
So 945026-41-5 is a valid CAS Registry Number.

945026-41-5Relevant articles and documents

Resolution of nitrogen-centered chiral tetraalkylammonium salts: application to [1,2] Stevens rearrangements with N-to-C chirality transmission

Tayama, Eiji,Otoyama, Seijun,Tanaka, Hiroyuki

experimental part, p. 2600 - 2608 (2010/03/24)

The resolution of N-chiral, amino acid-derived quaternary ammonium salts is demonstrated by using chiral BINOL as a complexing agent. Determination of the enantiopurities and absolute configurations of the resolved N-chiral tetraalkylammonium salts are described. The [1,2] Stevens rearrangement of N-chiral ammonium salts is shown to proceed with N-to-C chirality transmission to afford optically active 3-substituted morpholin-2-one derivatives.

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