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CAS

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1279712-43-4

2-tert-butyl 1-(2'-iodo-3'-methoxybenzyl) 3-methoxy-9,10-anthraquinone-1,2-dicarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1279712-43-4 Structure

  • Basic information

    1. Product Name: 2-tert-butyl 1-(2'-iodo-3'-methoxybenzyl) 3-methoxy-9,10-anthraquinone-1,2-dicarboxylate
    2. Synonyms: 2-tert-butyl 1-(2'-iodo-3'-methoxybenzyl) 3-methoxy-9,10-anthraquinone-1,2-dicarboxylate
    3. CAS NO:1279712-43-4
    4. Molecular Formula:
    5. Molecular Weight: 628.417
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1279712-43-4.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-tert-butyl 1-(2'-iodo-3'-methoxybenzyl) 3-methoxy-9,10-anthraquinone-1,2-dicarboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-tert-butyl 1-(2'-iodo-3'-methoxybenzyl) 3-methoxy-9,10-anthraquinone-1,2-dicarboxylate(1279712-43-4)
    11. EPA Substance Registry System: 2-tert-butyl 1-(2'-iodo-3'-methoxybenzyl) 3-methoxy-9,10-anthraquinone-1,2-dicarboxylate(1279712-43-4)

  • 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: 1279712-43-4(Hazardous Substances Data)

1279712-43-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1279712-43-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,7,9,7,1 and 2 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1279712-43:
(9*1)+(8*2)+(7*7)+(6*9)+(5*7)+(4*1)+(3*2)+(2*4)+(1*3)=184
184 % 10 = 4
So 1279712-43-4 is a valid CAS Registry Number.

1279712-43-4Relevant articles and documents

Total synthesis of cyclo-mumbaistatin analogues through anionic homo-fries rearrangement

Neufeind, Stefan,Huelsken, Nils,Neudoerfl, Joerg-Martin,Schloerer, Nils,Schmalz, Hans-Guenther

, p. 2633 - 2641 (2011/04/16)

The structurally unique polyketide mumbaistatin is the strongest naturally occurring inhibitor of glucose-6-phosphate translocase-1 (G6P-T1), which is a promising target for drugs against type-2 diabetes mellitus and angiogenic processes associated with brain tumor development. Despite its high relevance, mumbaistatin has so far withstood all attempts towards its total synthesis. In the present study an efficient total synthesis of a deoxy-mumbaistatin analogue containing the complete carbon skeleton and a spirolactone motif closely resembling the natural product in its cyclized form was elaborated. Key steps of the synthesis are a Diels-Alder cycloaddition for the construction of the fully functionalized anthraquinone moiety and an anionic homo-Fries rearrangement to build up the tetra-ortho-substituted benzophenone core motif, from which a spiroketal lactone forms in a spontaneous process. The elaborated strategy opens an entry to a variety of new analogs of mumbaistatin and cyclo-mumbaistatin and may be exploited for the total synthesis of the natural product itself in the future.

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