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CAS

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398136-45-3

2-benzyl-6-methoxyaniline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 398136-45-3 Structure

  • Basic information

    1. Product Name: 2-benzyl-6-methoxyaniline
    2. Synonyms: 2-benzyl-6-methoxyaniline
    3. CAS NO:398136-45-3
    4. Molecular Formula:
    5. Molecular Weight: 213.279
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 398136-45-3.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: 2-benzyl-6-methoxyaniline(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-benzyl-6-methoxyaniline(398136-45-3)
    11. EPA Substance Registry System: 2-benzyl-6-methoxyaniline(398136-45-3)

  • 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: 398136-45-3(Hazardous Substances Data)

398136-45-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 398136-45-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,8,1,3 and 6 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 398136-45:
(8*3)+(7*9)+(6*8)+(5*1)+(4*3)+(3*6)+(2*4)+(1*5)=183
183 % 10 = 3
So 398136-45-3 is a valid CAS Registry Number.

398136-45-3Relevant articles and documents

Chiral relay effect: 4-substituted 1,3-benzoxazol-2-(3H)-ones as achiral templates for enantioselective Diels-Alder reactions

Quaranta, Laura,Corminboeuf, Olivier,Renaud, Philippe

, p. 39 - 41 (2007/10/03)

(matrix presented) A new strategy to control the enantioselectivity of Lewis acid catalyzed reactions has been investigated. The use of N-acryloyl-1,3-benzoxazol-2-(3H)-ones substituted at position 4 leads to the formation of diastereomeric complexes as a

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