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56140-36-4

3-Methoxy-4-methyl-N,N-dimethylanilin is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 56140-36-4 Structure

  • Basic information

    1. Product Name: 3-Methoxy-4-methyl-N,N-dimethylanilin
    2. Synonyms:
    3. CAS NO:56140-36-4
    4. Molecular Formula:
    5. Molecular Weight: 165.235
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 56140-36-4.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-Methoxy-4-methyl-N,N-dimethylanilin(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-Methoxy-4-methyl-N,N-dimethylanilin(56140-36-4)
    11. EPA Substance Registry System: 3-Methoxy-4-methyl-N,N-dimethylanilin(56140-36-4)

  • 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: 56140-36-4(Hazardous Substances Data)

56140-36-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56140-36-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,1,4 and 0 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 56140-36:
(7*5)+(6*6)+(5*1)+(4*4)+(3*0)+(2*3)+(1*6)=104
104 % 10 = 4
So 56140-36-4 is a valid CAS Registry Number.

56140-36-4Downstream Products

56140-36-4Relevant articles and documents

Syntheses of Highly Substituted Benzenes via Diels-Alder Reactions with 2H-Pyran-2-ones

Ziegler, Thomas,Layh, Marcus,Effenberger, Franz

, p. 1347 - 1356 (2007/10/02)

The 2H-pyran-2-ones (α-pyrones) 1 react as dienes in Diels-Alder reactions with acetylene derivatives.The primarely formed cycloadducts immediately aromatize to benzenes by CO2 elimination.Thus, methyl acetylenedicarboxylate (2a) gives dimethyl phthalates 3, and methyl acetylenediphosphonate (2b) gives dimethyl 1,2-phenylenediphosphonates 8.The reactions of 1-(dimethylamino)-1-methoxyethene (9) with 1 regioselectively produce N,N-dimethylanilines 10 and isomeric homophthalate derivatives 12.Naphthoquinones 14 could be generated from 1,4-benzoquinone (13) and 1 in the presence of acetic anhydride and Pd/C.Hydroxy-2H-pyran-2-ones 4 react via their trimethylsilyl ether 6 analogously with 2a to give dimethyl (trimethylsiloxy)phthalates 7 which are easily converted to phenols 5 by acid-catalyzed hydrolysis.

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