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874758-26-6

2-iodo-1-trideuteriomethoxy-3-nitrobenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 874758-26-6 Structure

  • Basic information

    1. Product Name: 2-iodo-1-trideuteriomethoxy-3-nitrobenzene
    2. Synonyms: 2-iodo-1-trideuteriomethoxy-3-nitrobenzene
    3. CAS NO:874758-26-6
    4. Molecular Formula:
    5. Molecular Weight: 282.01
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 874758-26-6.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-iodo-1-trideuteriomethoxy-3-nitrobenzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-iodo-1-trideuteriomethoxy-3-nitrobenzene(874758-26-6)
    11. EPA Substance Registry System: 2-iodo-1-trideuteriomethoxy-3-nitrobenzene(874758-26-6)

  • 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: 874758-26-6(Hazardous Substances Data)

874758-26-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 874758-26-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,4,7,5 and 8 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 874758-26:
(8*8)+(7*7)+(6*4)+(5*7)+(4*5)+(3*8)+(2*2)+(1*6)=226
226 % 10 = 6
So 874758-26-6 is a valid CAS Registry Number.

874758-26-6Upstream product

874758-26-6Relevant articles and documents

Ortho effect in the Bergman cyclization: Interception of p-benzyne intermediate by intramolecular hydrogen abstraction

Zeidan, Tarek A.,Manoharan, Mariappan,Alabugin, Igor V.

, p. 954 - 961 (2006)

Intramolecular hydrogen atom (H-atom) abstraction from the o-OCH 3 group effectively intercepts the p-benzyne intermediate in the Bergman cycloaromatization of 2,3-diethynyl-1-methoxybenzene (1) before this intermediate undergoes either retro-Bergman ring opening or external H-atom abstraction. This process leads to the formation of a new diradical and renders the cyclization step essentially irreversible. Chemical and kinetic consequences of this phenomenon were investigated through the combination of computational and experimental studies.

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