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1428884-69-8

potassium trifluoro(1-((tert-butoxy)carbonyl)-1H-indol-3-yl)boranuide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1428884-69-8 Structure

  • Basic information

    1. Product Name: potassium trifluoro(1-((tert-butoxy)carbonyl)-1H-indol-3-yl)boranuide
    2. Synonyms: potassium trifluoro(1-((tert-butoxy)carbonyl)-1H-indol-3-yl)boranuide
    3. CAS NO:1428884-69-8
    4. Molecular Formula:
    5. Molecular Weight: 323.164
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1428884-69-8.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: potassium trifluoro(1-((tert-butoxy)carbonyl)-1H-indol-3-yl)boranuide(CAS DataBase Reference)
    10. NIST Chemistry Reference: potassium trifluoro(1-((tert-butoxy)carbonyl)-1H-indol-3-yl)boranuide(1428884-69-8)
    11. EPA Substance Registry System: potassium trifluoro(1-((tert-butoxy)carbonyl)-1H-indol-3-yl)boranuide(1428884-69-8)

  • 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: 1428884-69-8(Hazardous Substances Data)

1428884-69-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1428884-69-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,8,8,8 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1428884-69:
(9*1)+(8*4)+(7*2)+(6*8)+(5*8)+(4*8)+(3*4)+(2*6)+(1*9)=208
208 % 10 = 8
So 1428884-69-8 is a valid CAS Registry Number.

1428884-69-8Relevant articles and documents

A Total Synthesis of the Marine Alkaloid Discoipyrrole D

Zhang, Yiwen,Banwell, Martin G.

, p. 9328 - 9334 (2017)

A total synthesis of the diastereoisomeric pair of compounds, 4, assigned to the marine alkaloid discoipyrrole D is reported. A series of palladium-catalyzed cross-coupling and other reactions was employed to assemble the relevant 1,2,3,4-tetrasubstituted pyrrole (16) that was engaged in MoOPH-mediated oxidative cyclization, then conjugate addition, and redox processes to complete the synthesis. This work serves to confirm the structure (4) originally assigned to discoipyrrole D.

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