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1384277-16-0

N-[2-(1-(4-methoxybenzyl)-1H-indol-3-yl)ethyl]acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1384277-16-0 Structure

  • Basic information

    1. Product Name: N-[2-(1-(4-methoxybenzyl)-1H-indol-3-yl)ethyl]acetamide
    2. Synonyms: N-[2-(1-(4-methoxybenzyl)-1H-indol-3-yl)ethyl]acetamide
    3. CAS NO:1384277-16-0
    4. Molecular Formula:
    5. Molecular Weight: 322.407
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1384277-16-0.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: N-[2-(1-(4-methoxybenzyl)-1H-indol-3-yl)ethyl]acetamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-[2-(1-(4-methoxybenzyl)-1H-indol-3-yl)ethyl]acetamide(1384277-16-0)
    11. EPA Substance Registry System: N-[2-(1-(4-methoxybenzyl)-1H-indol-3-yl)ethyl]acetamide(1384277-16-0)

  • 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: 1384277-16-0(Hazardous Substances Data)

1384277-16-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1384277-16-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,4,2,7 and 7 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1384277-16:
(9*1)+(8*3)+(7*8)+(6*4)+(5*2)+(4*7)+(3*7)+(2*1)+(1*6)=180
180 % 10 = 0
So 1384277-16-0 is a valid CAS Registry Number.

1384277-16-0Downstream Products

1384277-16-0Relevant articles and documents

Synthesis of tryptamine derivatives via a direct, one-pot reductive alkylation of indoles

Righi, Marika,Topi, Francesca,Bartolucci, Silvia,Bedini, Annalida,Piersanti, Giovanni,Spadoni, Gilberto

experimental part, p. 6351 - 6357 (2012/10/08)

An efficient, one-pot reductive alkylation of indoles with N-protected aminoethyl acetals in the presence of TES/TFA is reported. It represents the first general method for the direct synthesis of tryptamine derivatives from indoles and nitrogen-functionalized acetals. This convergent and versatile approach employs safe and inexpensive reagents, proceeds under mild conditions, and tolerates several functional groups. The new procedure was efficiently applied to a gram-scale synthesis of both luzindole, a reference MT2-selective melatonin receptor antagonist, and melatonin.

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