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89102-04-5

Acetamide, N-[4-nitro-3-(phenylmethoxy)phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 89102-04-5 Structure

  • Basic information

    1. Product Name: Acetamide, N-[4-nitro-3-(phenylmethoxy)phenyl]-
    2. Synonyms:
    3. CAS NO:89102-04-5
    4. Molecular Formula: C15H14N2O4
    5. Molecular Weight: 286.287
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 89102-04-5.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: Acetamide, N-[4-nitro-3-(phenylmethoxy)phenyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Acetamide, N-[4-nitro-3-(phenylmethoxy)phenyl]-(89102-04-5)
    11. EPA Substance Registry System: Acetamide, N-[4-nitro-3-(phenylmethoxy)phenyl]-(89102-04-5)

  • 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: 89102-04-5(Hazardous Substances Data)

89102-04-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89102-04-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,1,0 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 89102-04:
(7*8)+(6*9)+(5*1)+(4*0)+(3*2)+(2*0)+(1*4)=125
125 % 10 = 5
So 89102-04-5 is a valid CAS Registry Number.

89102-04-5Relevant articles and documents

SYNTHESIS AND INTRAMOLECULAR PHOTOADDITION OF AN INDOLE QUINONEDIAZIDE

Sundberg, Richard J.,Nishiguchi, Takeshi

, p. 4773 - 4776 (2007/10/02)

An intramolecular carbenoid photoaddition route to the unique spiro-cyclopropane indol-7-one ring system of the antibiotic CC-1065 has been explored.The diazo transfer reaction of a 7-hydroxyindole intermediate leads via a 6-diazo intermediate to an isome

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