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methyl 2-(N-tosyl-1-cyano-1,2-dihydro-5,6,7-trimethoxy-8-isoquinolyl)acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 91523-17-0 Structure
  • Basic information

    1. Product Name: methyl 2-(N-tosyl-1-cyano-1,2-dihydro-5,6,7-trimethoxy-8-isoquinolyl)acetate
    2. Synonyms: methyl 2-(N-tosyl-1-cyano-1,2-dihydro-5,6,7-trimethoxy-8-isoquinolyl)acetate
    3. CAS NO:91523-17-0
    4. Molecular Formula:
    5. Molecular Weight: 472.519
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 91523-17-0.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: methyl 2-(N-tosyl-1-cyano-1,2-dihydro-5,6,7-trimethoxy-8-isoquinolyl)acetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 2-(N-tosyl-1-cyano-1,2-dihydro-5,6,7-trimethoxy-8-isoquinolyl)acetate(91523-17-0)
    11. EPA Substance Registry System: methyl 2-(N-tosyl-1-cyano-1,2-dihydro-5,6,7-trimethoxy-8-isoquinolyl)acetate(91523-17-0)
  • 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: 91523-17-0(Hazardous Substances Data)

91523-17-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91523-17-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,5,2 and 3 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 91523-17:
(7*9)+(6*1)+(5*5)+(4*2)+(3*3)+(2*1)+(1*7)=120
120 % 10 = 0
So 91523-17-0 is a valid CAS Registry Number.

91523-17-0Downstream Products

91523-17-0Relevant articles and documents

Total synthesis of granditropone, grandirubrine, imerubrine, and isoimerubrine

Boger, Dale L.,Takahashi, Kanji

, p. 12452 - 12459 (2007/10/03)

Concise total syntheses of the naturally occurring tropoloisoquinolines grandirubrine (1), imerubrine (2), and isoimerubrine (3) are detailed. The regioselective total synthesis of grandirubrine (1) is based on the [4 + 2]cycloaddition reaction of the α-p

Total Syntheses of Azafluoranthene Alkaloids: Rufescine and Imeluteine

Boger, Dale L.,Brotherton, Christine E.

, p. 4050 - 4055 (2007/10/02)

Total syntheses of rufescine and imeluteine, azafluoranthene alkaloids isolated from Abuta imene and Abuta rufescens, are detailed and are based on the utilization of the inverse electron demand Diels-Alder reactions of 3-carbomethoxy-2-pyrones for the selective and controlled introduction of oxygenated aromatics.

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