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201225-31-2

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

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  • 201225-31-2 Structure

  • Basic information

    1. Product Name: 2-Chloro-N-[2-(1H-indol-3-yl)-ethyl]-N-(4-oxo-cyclohexyl)-acetamide
    2. Synonyms: 2-Chloro-N-[2-(1H-indol-3-yl)-ethyl]-N-(4-oxo-cyclohexyl)-acetamide
    3. CAS NO:201225-31-2
    4. Molecular Formula:
    5. Molecular Weight: 332.83
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 201225-31-2.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: 2-Chloro-N-[2-(1H-indol-3-yl)-ethyl]-N-(4-oxo-cyclohexyl)-acetamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Chloro-N-[2-(1H-indol-3-yl)-ethyl]-N-(4-oxo-cyclohexyl)-acetamide(201225-31-2)
    11. EPA Substance Registry System: 2-Chloro-N-[2-(1H-indol-3-yl)-ethyl]-N-(4-oxo-cyclohexyl)-acetamide(201225-31-2)

  • 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: 201225-31-2(Hazardous Substances Data)

201225-31-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 201225-31-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,1,2,2 and 5 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 201225-31:
(8*2)+(7*0)+(6*1)+(5*2)+(4*2)+(3*5)+(2*3)+(1*1)=62
62 % 10 = 2
So 201225-31-2 is a valid CAS Registry Number.

201225-31-2Relevant articles and documents

First Total Synthesis of (±)-Melinonine-E and (i)-Strychnoxanthine Using a Radical Cyclization Process as the Core Ring-Forming Step

Quirante, Josefina,Escolano, Carmen,Merino, Alma,Bonjoch, Josep

, p. 968 - 976 (1998)

The first total synthesis of (±)-melinonine-E and (±)-strychnoxanthine is described. The key common step for the synthesis of both alkaloids is the elaboration of the 2-azabicyclo[3.3.1]nonane nucleus (D and E rings) by a radical carbocyclization, using an α-carbamoyldichloromethyl radical as a donor. The closure of the C ring by a Bischler-Napieralski cyclization, followed by an epimerization process to gain the axial nitrile 20, and appropriate reduction transformations afforded pentacyclic alcohol 23. This alcohol was converted into either (±)-melinonine-E (1) or (±)-strychnoxanthine (2) by means of a palladium black dehydrogenation of the C ring or a SeO2 oxidation of the corresponding acetate 25, respectively.

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