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2-(6-Isopropoxy-7-methoxy-1-oxo-1,2,3,4-tetrahydro-naphthalen-2-yl)-3,4,5-trimethoxy-benzoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 98799-68-9 Structure
  • Basic information

    1. Product Name: 2-(6-Isopropoxy-7-methoxy-1-oxo-1,2,3,4-tetrahydro-naphthalen-2-yl)-3,4,5-trimethoxy-benzoic acid
    2. Synonyms:
    3. CAS NO:98799-68-9
    4. Molecular Formula:
    5. Molecular Weight: 444.482
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 98799-68-9.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-(6-Isopropoxy-7-methoxy-1-oxo-1,2,3,4-tetrahydro-naphthalen-2-yl)-3,4,5-trimethoxy-benzoic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(6-Isopropoxy-7-methoxy-1-oxo-1,2,3,4-tetrahydro-naphthalen-2-yl)-3,4,5-trimethoxy-benzoic acid(98799-68-9)
    11. EPA Substance Registry System: 2-(6-Isopropoxy-7-methoxy-1-oxo-1,2,3,4-tetrahydro-naphthalen-2-yl)-3,4,5-trimethoxy-benzoic acid(98799-68-9)
  • 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: 98799-68-9(Hazardous Substances Data)

98799-68-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98799-68-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,7,9 and 9 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 98799-68:
(7*9)+(6*8)+(5*7)+(4*9)+(3*9)+(2*6)+(1*8)=229
229 % 10 = 9
So 98799-68-9 is a valid CAS Registry Number.

98799-68-9Downstream Products

98799-68-9Relevant articles and documents

Direct Synthesis of Benzophenanthridines and Benzophenanthridones via SRN1 Reactions

Beugelmans, Rene,Chastanet, Jacqueline,Ginsburg, Helene,Quintero-Cortes, Leticia,Roussi, Georges

, p. 4933 - 4938 (2007/10/02)

A straightforward and high-yield route to the 11,12-dihydrobenzophenanthridine (3) and 11,12-dihydrobenzophenanthridone (14) ring systems is based upon an SRN1 reaction between 2-halobenzylamines 1 or 2-halobenzoic acids 11 and enolates derived from tetralones 2.The efficient dehydrogenation of 3 or 14 gives the benzophenthridines 4 or benzophenanthridones 15.Use of properly substituted reactants leads to nitidine, avicine, and fagaronine and to analogues of those natural products.

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