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2-(2,3-diiodophenoxy)-2-methylpropanamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1287791-71-2 Structure
  • Basic information

    1. Product Name: 2-(2,3-diiodophenoxy)-2-methylpropanamide
    2. Synonyms: 2-(2,3-diiodophenoxy)-2-methylpropanamide
    3. CAS NO:1287791-71-2
    4. Molecular Formula:
    5. Molecular Weight: 431.012
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1287791-71-2.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-(2,3-diiodophenoxy)-2-methylpropanamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(2,3-diiodophenoxy)-2-methylpropanamide(1287791-71-2)
    11. EPA Substance Registry System: 2-(2,3-diiodophenoxy)-2-methylpropanamide(1287791-71-2)
  • 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: 1287791-71-2(Hazardous Substances Data)

1287791-71-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1287791-71-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,8,7,7,9 and 1 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1287791-71:
(9*1)+(8*2)+(7*8)+(6*7)+(5*7)+(4*9)+(3*1)+(2*7)+(1*1)=212
212 % 10 = 2
So 1287791-71-2 is a valid CAS Registry Number.

1287791-71-2Relevant articles and documents

Approaches to the synthesis of 2,3-dihaloanilines. Useful precursors of 4-functionalized-1 H-indoles

Guilarte, Veronica,Castroviejo, M. Pilar,Garcia-Garcia, Patricia,Fernandez-Rodriguez, Manuel A.,Sanz, Roberto

, p. 3416 - 3437 (2011/06/28)

2,3-Dihaloanilines have been proved as useful starting materials for synthesizing 4-halo-1H-indoles. Subsequent or in situ functionalization of the prepared haloindoles allows the access to a wide variety of 2,4- or 2,3,4-regioselectively functionalized indoles in good overall yields. As no efficient synthetic routes to 2,3-dihaloanilines have been described in the literature, different approaches to the preparation of these 1,2,3-functionalized aromatic precursors are now presented. The most general one involves a Smiles rearrangement from the corresponding 2,3-dihalophenols and allows the preparation of 2,3-dihaloanilides in a straightforward and synthetically useful manner.

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