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65037-64-1

1H-Indole, 3,3'-(1,1-dimethyl-3-methylene-1,3-propanediyl)bis[1-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 65037-64-1 Structure

  • Basic information

    1. Product Name: 1H-Indole, 3,3'-(1,1-dimethyl-3-methylene-1,3-propanediyl)bis[1-methyl-
    2. Synonyms:
    3. CAS NO:65037-64-1
    4. Molecular Formula: C24H26N2
    5. Molecular Weight: 342.484
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 65037-64-1.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: 1H-Indole, 3,3'-(1,1-dimethyl-3-methylene-1,3-propanediyl)bis[1-methyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1H-Indole, 3,3'-(1,1-dimethyl-3-methylene-1,3-propanediyl)bis[1-methyl-(65037-64-1)
    11. EPA Substance Registry System: 1H-Indole, 3,3'-(1,1-dimethyl-3-methylene-1,3-propanediyl)bis[1-methyl-(65037-64-1)

  • 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: 65037-64-1(Hazardous Substances Data)

65037-64-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65037-64-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,0,3 and 7 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 65037-64:
(7*6)+(6*5)+(5*0)+(4*3)+(3*7)+(2*6)+(1*4)=121
121 % 10 = 1
So 65037-64-1 is a valid CAS Registry Number.

65037-64-1Downstream Products

65037-64-1Relevant articles and documents

New Reactions of 3-Vinyl- and 3-(2-Propenyl)indoles with N- Phenylmaleimide: Cycloaddition, Ene Reaction, and Dimerization

Pfeuffer, Ludwig,Pindur, Ulf

, p. 467 - 471 (1988)

Depending on the substitution pattern of the aminobutadiene subunit in the selected 3-vinylindoles 1, 3, 6, and 9, stereospecific cycloadditions ("endo"-preference) and dimerizations take place on reaction with N- phenylmaleimide.In the reaction of 9 with N-phenylmaleimide in the absence of a Lewis-acid catalyst, a competing ene reaction occurs in addition to the Diels-Alder reaction.

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