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190182-62-8

3-(diethylaminomethyl)-5-benzyloxyindol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 190182-62-8 Structure

  • Basic information

    1. Product Name: 3-(diethylaminomethyl)-5-benzyloxyindol
    2. Synonyms: 3-(diethylaminomethyl)-5-benzyloxyindol
    3. CAS NO:190182-62-8
    4. Molecular Formula:
    5. Molecular Weight: 308.423
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 190182-62-8.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: 3-(diethylaminomethyl)-5-benzyloxyindol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(diethylaminomethyl)-5-benzyloxyindol(190182-62-8)
    11. EPA Substance Registry System: 3-(diethylaminomethyl)-5-benzyloxyindol(190182-62-8)

  • 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: 190182-62-8(Hazardous Substances Data)

190182-62-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 190182-62-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,0,1,8 and 2 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 190182-62:
(8*1)+(7*9)+(6*0)+(5*1)+(4*8)+(3*2)+(2*6)+(1*2)=128
128 % 10 = 8
So 190182-62-8 is a valid CAS Registry Number.

190182-62-8Relevant articles and documents

Synthesis of 3-Amino-2-(3-indolyl)propanol and propanoate derivatives and preliminary cardiovascular evaluation in rats

Perez-Alvarez, Victor,Morales-Rios, Martha S.,Hong, Enrique,Joseph-Nathan, Pedro

, p. 246 - 252 (2007/10/03)

A series of tryptamine analogues has been prepared and tested for their 5-HT1 receptor agonist properties. The incorporation of an alkoxy group at the C-5 position of the indole nucleus resulted in a short-lived and dose-dependent immediate ant

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