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CAS

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494803-91-7

N-[2-(1-benzenesulfonyl-1H-indol-3-yl)-2-hydroxy-ethyl]-2-methylamino-3-phenyl-propionamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 494803-91-7 Structure

  • Basic information

    1. Product Name: N-[2-(1-benzenesulfonyl-1H-indol-3-yl)-2-hydroxy-ethyl]-2-methylamino-3-phenyl-propionamide
    2. Synonyms: N-[2-(1-benzenesulfonyl-1H-indol-3-yl)-2-hydroxy-ethyl]-2-methylamino-3-phenyl-propionamide
    3. CAS NO:494803-91-7
    4. Molecular Formula:
    5. Molecular Weight: 477.584
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 494803-91-7.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-benzenesulfonyl-1H-indol-3-yl)-2-hydroxy-ethyl]-2-methylamino-3-phenyl-propionamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-[2-(1-benzenesulfonyl-1H-indol-3-yl)-2-hydroxy-ethyl]-2-methylamino-3-phenyl-propionamide(494803-91-7)
    11. EPA Substance Registry System: N-[2-(1-benzenesulfonyl-1H-indol-3-yl)-2-hydroxy-ethyl]-2-methylamino-3-phenyl-propionamide(494803-91-7)

  • 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: 494803-91-7(Hazardous Substances Data)

494803-91-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 494803-91-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,4,8,0 and 3 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 494803-91:
(8*4)+(7*9)+(6*4)+(5*8)+(4*0)+(3*3)+(2*9)+(1*1)=187
187 % 10 = 7
So 494803-91-7 is a valid CAS Registry Number.

494803-91-7Relevant articles and documents

A short synthesis of aspergillamide B. The marine natural product from Aspergillus sp.

Rivas, Lucrecia,Quintero, Leticia,Fourrey, Jean-Louis,Benhida, Rachid

, p. 7639 - 7641 (2007/10/03)

A short route to the marine natural product aspergillamide B has been developed. The key step is the stereoselective formation of the trans indole-enamide pharmacophore by indole-assisted dehydration from the functionalized aminoalcohol intermediate. HPLC and 1H NMR analyses show that aspergillamide B is more stable in the cis rotamer form.

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