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1608150-20-4

ethyl (2S,4S,6S)-4,6-bis(7-methyl-1H-indol-3-yl)-1-phenylpiperidine-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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  • 1608150-20-4 Structure

  • Basic information

    1. Product Name: ethyl (2S,4S,6S)-4,6-bis(7-methyl-1H-indol-3-yl)-1-phenylpiperidine-2-carboxylate
    2. Synonyms:
    3. CAS NO:1608150-20-4
    4. Molecular Formula:
    5. Molecular Weight: 491.633
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1608150-20-4.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: ethyl (2S,4S,6S)-4,6-bis(7-methyl-1H-indol-3-yl)-1-phenylpiperidine-2-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl (2S,4S,6S)-4,6-bis(7-methyl-1H-indol-3-yl)-1-phenylpiperidine-2-carboxylate(1608150-20-4)
    11. EPA Substance Registry System: ethyl (2S,4S,6S)-4,6-bis(7-methyl-1H-indol-3-yl)-1-phenylpiperidine-2-carboxylate(1608150-20-4)

  • 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: 1608150-20-4(Hazardous Substances Data)

1608150-20-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1608150-20-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,8,1,5 and 0 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1608150-20:
(9*1)+(8*6)+(7*0)+(6*8)+(5*1)+(4*5)+(3*0)+(2*2)+(1*0)=134
134 % 10 = 4
So 1608150-20-4 is a valid CAS Registry Number.

1608150-20-4Downstream Products

1608150-20-4Relevant articles and documents

Asymmetric organocatalytic synthesis of 4,6-bis(1H-indole-3-yl)-piperidine- 2 carboxylates

Zhong, Sabilla,Nieger, Martin,Bihlmeier, Angela,Shi, Min,Braese, Stefan

, p. 3265 - 3270 (2014/05/06)

We developed an asymmetric organocatalytic synthesis of 4,6-bis(1H-indole-3-yl)-piperidine-2-carboxylates using 10 mol% of a chiral phosphoric acid. The products, which are novel bisindole-piperidine-amino acid hybrids, can be obtained in one step from 3-

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