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220966-22-3

2-(2-bromo-4-chloro-phenoxymethyl)-isoindole-1,3-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 220966-22-3 Structure

  • Basic information

    1. Product Name: 2-(2-bromo-4-chloro-phenoxymethyl)-isoindole-1,3-dione
    2. Synonyms: 2-(2-bromo-4-chloro-phenoxymethyl)-isoindole-1,3-dione
    3. CAS NO:220966-22-3
    4. Molecular Formula:
    5. Molecular Weight: 366.598
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 220966-22-3.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-(2-bromo-4-chloro-phenoxymethyl)-isoindole-1,3-dione(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(2-bromo-4-chloro-phenoxymethyl)-isoindole-1,3-dione(220966-22-3)
    11. EPA Substance Registry System: 2-(2-bromo-4-chloro-phenoxymethyl)-isoindole-1,3-dione(220966-22-3)

  • 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: 220966-22-3(Hazardous Substances Data)

220966-22-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 220966-22-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,9,6 and 6 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 220966-22:
(8*2)+(7*2)+(6*0)+(5*9)+(4*6)+(3*6)+(2*2)+(1*2)=123
123 % 10 = 3
So 220966-22-3 is a valid CAS Registry Number.

220966-22-3Relevant articles and documents

Synthesis of isoindolo[1,3]benzoxazine derivatives through intramolecular arylation of N-acyliminium ions

Hucher, Nicolas,Daich, Adam,Decroix, Bernard

, p. 1477 - 1483 (1998)

[1,3]Benzoxazines annulated to isoindole as 3 and 4 have been synthesized in three steps from N-chloromethylphthalimide 5 and substituted phenols 6. The key step was the acid-catalyzed cyclization of ω-carbinol lactams 8 and 9.

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