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1374411-76-3

C23H27NO4 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1374411-76-3 Structure

  • Basic information

    1. Product Name: C23H27NO4
    2. Synonyms:
    3. CAS NO:1374411-76-3
    4. Molecular Formula:
    5. Molecular Weight: 381.472
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1374411-76-3.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: C23H27NO4(CAS DataBase Reference)
    10. NIST Chemistry Reference: C23H27NO4(1374411-76-3)
    11. EPA Substance Registry System: C23H27NO4(1374411-76-3)

  • 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: 1374411-76-3(Hazardous Substances Data)

1374411-76-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1374411-76-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,4,4,1 and 1 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1374411-76:
(9*1)+(8*3)+(7*7)+(6*4)+(5*4)+(4*1)+(3*1)+(2*7)+(1*6)=153
153 % 10 = 3
So 1374411-76-3 is a valid CAS Registry Number.

1374411-76-3Downstream Products

1374411-76-3Relevant articles and documents

Enantioselective annulation reactions of bisenolates prepared through dearomatization reactions of aromatic and heteroaromatic diesters

Perez-Vazquez, Jaime,Veiga, Alberte X.,Prado, Gustavo,Sardina, F. Javier,Paleo, M. Rita

, p. 975 - 987 (2012/04/04)

A one-pot, enantioselective strategy for the dearomatization-annulation of aromatic diesters to give a range of highly functionalized polycyclic molecules with excellent enantioselectivity is presented. This methodology is based on the reaction of bisenolates, prepared by treating aromatic diesters with trialkyltin lithium reagents, which involves a stanna-Brook rearrangement, with 1,ω-dihaloalkanes and other biselectrophiles. We have also developed experimental conditions for performing these reactions with substoichiometric amounts of the required tin reagent by in situ recycling of Me 6Sn2 into Me3SnLi with excess lithium metal, and provide a study of the scope and limitations of this synthetic methodology. The alkylation of chiral bisenolates opens a straightforward one-pot access to highly functionalized bicyclic compounds from aromatic diesters. A stanna-Brook rearrangement originates the key bisenolate intermediate. Copyright

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