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1373442-44-4

(E)-4-bromo-2-(3-methoxy-3-oxoprop-1-en-1-yl)benzene-1-diazonium tetrafluoroborate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1373442-44-4 Structure

  • Basic information

    1. Product Name: (E)-4-bromo-2-(3-methoxy-3-oxoprop-1-en-1-yl)benzene-1-diazonium tetrafluoroborate
    2. Synonyms: (E)-4-bromo-2-(3-methoxy-3-oxoprop-1-en-1-yl)benzene-1-diazonium tetrafluoroborate
    3. CAS NO:1373442-44-4
    4. Molecular Formula:
    5. Molecular Weight: 354.894
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1373442-44-4.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: (E)-4-bromo-2-(3-methoxy-3-oxoprop-1-en-1-yl)benzene-1-diazonium tetrafluoroborate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-4-bromo-2-(3-methoxy-3-oxoprop-1-en-1-yl)benzene-1-diazonium tetrafluoroborate(1373442-44-4)
    11. EPA Substance Registry System: (E)-4-bromo-2-(3-methoxy-3-oxoprop-1-en-1-yl)benzene-1-diazonium tetrafluoroborate(1373442-44-4)

  • 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: 1373442-44-4(Hazardous Substances Data)

1373442-44-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1373442-44-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,3,4,4 and 2 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1373442-44:
(9*1)+(8*3)+(7*7)+(6*3)+(5*4)+(4*4)+(3*2)+(2*4)+(1*4)=154
154 % 10 = 4
So 1373442-44-4 is a valid CAS Registry Number.

1373442-44-4Relevant articles and documents

Selective arene functionalization through sequential oxidative and non-oxidative Heck reactions

Schmidt, Bernd,Elizarov, Nelli

, p. 4350 - 4352 (2012)

A sequence of acetamide directed oxidative Heck reaction and deacetylation-diazotation-Heck coupling allows the traceless removal of the acetamide group and its dual exploitation as a catalyst directing group and a leaving group. The Royal Society of Chem

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