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CAS

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1432581-91-3

(S)-methyl 3-benzyl-4-oxo-6-pentyl-2,3,4,7-tetrahydro-1H-azocino[5,4-b]indole-2-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1432581-91-3 Structure

  • Basic information

    1. Product Name: (S)-methyl 3-benzyl-4-oxo-6-pentyl-2,3,4,7-tetrahydro-1H-azocino[5,4-b]indole-2-carboxylate
    2. Synonyms:
    3. CAS NO:1432581-91-3
    4. Molecular Formula:
    5. Molecular Weight: 430.547
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1432581-91-3.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: (S)-methyl 3-benzyl-4-oxo-6-pentyl-2,3,4,7-tetrahydro-1H-azocino[5,4-b]indole-2-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-methyl 3-benzyl-4-oxo-6-pentyl-2,3,4,7-tetrahydro-1H-azocino[5,4-b]indole-2-carboxylate(1432581-91-3)
    11. EPA Substance Registry System: (S)-methyl 3-benzyl-4-oxo-6-pentyl-2,3,4,7-tetrahydro-1H-azocino[5,4-b]indole-2-carboxylate(1432581-91-3)

  • 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: 1432581-91-3(Hazardous Substances Data)

1432581-91-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1432581-91-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,3,2,5,8 and 1 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1432581-91:
(9*1)+(8*4)+(7*3)+(6*2)+(5*5)+(4*8)+(3*1)+(2*9)+(1*1)=153
153 % 10 = 3
So 1432581-91-3 is a valid CAS Registry Number.

1432581-91-3Downstream Products

1432581-91-3Relevant articles and documents

Synthesis of azocino[5,4-b]indoles via gold-catalyzed intramolecular alkyne hydroarylation

Peshkov, Vsevolod A.,Pereshivko, Olga P.,Der Eycken, Erik V. Van

, p. 2841 - 2848 (2013/01/15)

An efficient procedure for the synthesis of the azocinoACHTUNGTRENUNG[5,4- b]indole framework is presented, relying on a cationic gold-catalyzed intramolecular alkyne hydroarylation of propargylic amides derived from various tryptamines and 3-substituted

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