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α-ethyl-5-methyl-9-methylene-12-benzyl-6,7,8,9,10,11-hexahydro-6,10-imino-5H-cyclooctindole-8-acetaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

122490-94-2

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  • 122490-94-2 Structure

  • Basic information

    1. Product Name: α-ethyl-5-methyl-9-methylene-12-benzyl-6,7,8,9,10,11-hexahydro-6,10-imino-5H-cyclooctindole-8-acetaldehyde
    2. Synonyms:
    3. CAS NO:122490-94-2
    4. Molecular Formula:
    5. Molecular Weight: 398.548
    6. EINECS: N/A
    7. Product Categories: N/A

  • 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: α-ethyl-5-methyl-9-methylene-12-benzyl-6,7,8,9,10,11-hexahydro-6,10-imino-5H-cyclooctindole-8-acetaldehyde(CAS DataBase Reference)
    10. NIST Chemistry Reference: α-ethyl-5-methyl-9-methylene-12-benzyl-6,7,8,9,10,11-hexahydro-6,10-imino-5H-cyclooctindole-8-acetaldehyde(122490-94-2)
    11. EPA Substance Registry System: α-ethyl-5-methyl-9-methylene-12-benzyl-6,7,8,9,10,11-hexahydro-6,10-imino-5H-cyclooctindole-8-acetaldehyde(122490-94-2)

  • 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: 122490-94-2(Hazardous Substances Data)

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122490-94-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 122490-94-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,4,9 and 0 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 122490-94:
(8*1)+(7*2)+(6*2)+(5*4)+(4*9)+(3*0)+(2*9)+(1*4)=112
112 % 10 = 2
So 122490-94-2 is a valid CAS Registry Number.

122490-94-2Relevant academic research and scientific papers

Pictet-Spengler reactions in aprotic media. The total synthesis of (±) suaveoline

Trudell,Soerens,Weber,Hutchins,Grubisha,Bennett,Cook

, p. 1805 - 1822 (2007/10/02)

The first total synthesis of the indole alkaloid (±)-suaveoline 1 (a macroline-related base and a member of the sarpagine/ajmaline class of alkaloids) was completed in a stereocontrolled fashion. The serial synthesis employed three intramolecular reaction

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