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1247072-51-0

C22H25F3N2O3Si is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1247072-51-0 Structure

  • Basic information

    1. Product Name: C22H25F3N2O3Si
    2. Synonyms:
    3. CAS NO:1247072-51-0
    4. Molecular Formula:
    5. Molecular Weight: 450.533
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1247072-51-0.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: C22H25F3N2O3Si(CAS DataBase Reference)
    10. NIST Chemistry Reference: C22H25F3N2O3Si(1247072-51-0)
    11. EPA Substance Registry System: C22H25F3N2O3Si(1247072-51-0)

  • 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: 1247072-51-0(Hazardous Substances Data)

1247072-51-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1247072-51-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,7,0,7 and 2 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1247072-51:
(9*1)+(8*2)+(7*4)+(6*7)+(5*0)+(4*7)+(3*2)+(2*5)+(1*1)=140
140 % 10 = 0
So 1247072-51-0 is a valid CAS Registry Number.

1247072-51-0Downstream Products

1247072-51-0Relevant articles and documents

Regioselective oxidative arylation of indoles bearing N-alkyl protecting groups: Dual c-h functionalization via a concerted metalation-deprotonation mechanism

Potavathri, Shathaverdhan,Pereira, Kyle C.,Gorelsky, Serge I.,Pike, Andrew,Lebris, Alexis P.,Deboef, Brenton

supporting information; experimental part, p. 14676 - 14681 (2010/12/24)

The most direct method for synthesizing 2-arylindoles is oxidative coupling of an arene with an indole. We have shown that both the activity and regioselectivity of this cross-coupling reaction are correlated with the acidity of the medium. This insight has been applied to predict the best conditions for the oxidative cross-coupling of N-alkylindoles, an important class of substrates that has heretofore been incompatible with the harsh conditions required for oxidative cross-coupling. Both experimental and computational data indicate that the mechanism for C-H palladation of both the indoles and simple arenes is best described as concerted metalation-deprotonation, regardless of the substitution on the arene.

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