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CAS

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132619-30-8

(-)-1-Benzoyl-1,2,2a,3,4,5-hexahydrobenzindol-4-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 132619-30-8 Structure

  • Basic information

    1. Product Name: (-)-1-Benzoyl-1,2,2a,3,4,5-hexahydrobenzindol-4-amine
    2. Synonyms: (-)-1-Benzoyl-1,2,2a,3,4,5-hexahydrobenzindol-4-amine
    3. CAS NO:132619-30-8
    4. Molecular Formula:
    5. Molecular Weight: 278.354
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 132619-30-8.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: (-)-1-Benzoyl-1,2,2a,3,4,5-hexahydrobenzindol-4-amine(CAS DataBase Reference)
    10. NIST Chemistry Reference: (-)-1-Benzoyl-1,2,2a,3,4,5-hexahydrobenzindol-4-amine(132619-30-8)
    11. EPA Substance Registry System: (-)-1-Benzoyl-1,2,2a,3,4,5-hexahydrobenzindol-4-amine(132619-30-8)

  • 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: 132619-30-8(Hazardous Substances Data)

132619-30-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132619-30-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,6,1 and 9 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 132619-30:
(8*1)+(7*3)+(6*2)+(5*6)+(4*1)+(3*9)+(2*3)+(1*0)=108
108 % 10 = 8
So 132619-30-8 is a valid CAS Registry Number.

132619-30-8Relevant articles and documents

THE SYNTHESIS OF (+)- AND (-)-1-BENZOYL-1,2,2a,3,4,5-HEXAHYDROBENZINDOL-4-AMINE, and PREPARATION OF LY228729

Martinelli, Michael J.,Leanna, M. Robert,Varie, David L.,Peterson, Barry C.,Kress, Thomas J.,et al.

, p. 7579 - 7582 (1990)

Racemic epoxide 5 was reacted with S-Phenylethylamine to afford diastereomers 6 and 7, from which amino alcohol 6 could be isolated directly.Aziridine formation and tandem-hydrogenolysis provided optically pure primary amine 2 (31percent from racemic 4),

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