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107020-25-7

2,3,4,9-tetrahydro-2-(2-methoxy-3-methoxycarbonylbenzoyl)-1-methylene-1H-pyrido<3,4-b>indole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 107020-25-7 Structure

  • Basic information

    1. Product Name: 2,3,4,9-tetrahydro-2-(2-methoxy-3-methoxycarbonylbenzoyl)-1-methylene-1H-pyrido<3,4-b>indole
    2. Synonyms:
    3. CAS NO:107020-25-7
    4. Molecular Formula:
    5. Molecular Weight: 376.412
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 107020-25-7.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: 2,3,4,9-tetrahydro-2-(2-methoxy-3-methoxycarbonylbenzoyl)-1-methylene-1H-pyrido<3,4-b>indole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,3,4,9-tetrahydro-2-(2-methoxy-3-methoxycarbonylbenzoyl)-1-methylene-1H-pyrido<3,4-b>indole(107020-25-7)
    11. EPA Substance Registry System: 2,3,4,9-tetrahydro-2-(2-methoxy-3-methoxycarbonylbenzoyl)-1-methylene-1H-pyrido<3,4-b>indole(107020-25-7)

  • 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: 107020-25-7(Hazardous Substances Data)

107020-25-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107020-25-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,0,2 and 0 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 107020-25:
(8*1)+(7*0)+(6*7)+(5*0)+(4*2)+(3*0)+(2*2)+(1*5)=67
67 % 10 = 7
So 107020-25-7 is a valid CAS Registry Number.

107020-25-7Downstream Products

107020-25-7Relevant articles and documents

Photocyclization of enamides. XXXIV. A practical total synthesis of aromatic yohimboid alkaloids, oxogambirtannine and naucleficine

Naito,Kuroda,Miyata,Ninomiya

, p. 2216 - 2218 (2007/10/02)

Total synthesis of naucleficine (3a) was accomplished for the first time via an alkaloid, oxogambirtannine (3b), which was efficiently prepared by photocyclization of the o-methoxy-enamide 2b. The method is a practical one, suitable for large-scale preparation.

TOTAL SYNTHESIS OF NAUCLEA ALKALOID NAUCLEFICINE

Naito, Takeaki,Doi, Etsuko,Miyata, Okiko,Ninomiya, Ichiya

, p. 903 - 906 (2007/10/02)

The first total synthesis of naucleficine (1), an alkaloid of Nauclea officinalis, was achieved according to the route involving enamide photocyclization.

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