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CAS

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214615-05-1

3-(4-methoxybenzyl)indoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 214615-05-1 Structure

  • Basic information

    1. Product Name: 3-(4-methoxybenzyl)indoline
    2. Synonyms: 3-(4-methoxybenzyl)indoline
    3. CAS NO:214615-05-1
    4. Molecular Formula:
    5. Molecular Weight: 239.317
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 214615-05-1.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-(4-methoxybenzyl)indoline(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(4-methoxybenzyl)indoline(214615-05-1)
    11. EPA Substance Registry System: 3-(4-methoxybenzyl)indoline(214615-05-1)

  • 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: 214615-05-1(Hazardous Substances Data)

214615-05-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 214615-05-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,4,6,1 and 5 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 214615-05:
(8*2)+(7*1)+(6*4)+(5*6)+(4*1)+(3*5)+(2*0)+(1*5)=101
101 % 10 = 1
So 214615-05-1 is a valid CAS Registry Number.

214615-05-1Downstream Products

214615-05-1Relevant articles and documents

Hydrogenation or Dehydrogenation of N-Containing Heterocycles Catalyzed by a Single Manganese Complex

Borghs, Jannik C.,Rueping, Magnus,Zubar, Viktoriia

, (2020)

A highly chemoselective base-metal catalyzed hydrogenation and acceptorless dehydrogenation of N-heterocycles is presented. A well-defined Mn complex operates at low catalyst loading (as low as 2 mol %) and under mild reaction conditions. The described catalytic system tolerates various functional groups, and the corresponding reduced heterocycles can be obtained in high yields. Experimental studies indicate a metal-ligand cooperative catalysis mechanism.

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