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1245795-62-3

ethyl 4-(difluoromethoxy)-2-(pivalamido)phenylcarbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1245795-62-3 Structure

  • Basic information

    1. Product Name: ethyl 4-(difluoromethoxy)-2-(pivalamido)phenylcarbamate
    2. Synonyms: ethyl 4-(difluoromethoxy)-2-(pivalamido)phenylcarbamate
    3. CAS NO:1245795-62-3
    4. Molecular Formula:
    5. Molecular Weight: 330.332
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1245795-62-3.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: ethyl 4-(difluoromethoxy)-2-(pivalamido)phenylcarbamate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 4-(difluoromethoxy)-2-(pivalamido)phenylcarbamate(1245795-62-3)
    11. EPA Substance Registry System: ethyl 4-(difluoromethoxy)-2-(pivalamido)phenylcarbamate(1245795-62-3)

  • 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: 1245795-62-3(Hazardous Substances Data)

1245795-62-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1245795-62-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,5,7,9 and 5 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1245795-62:
(9*1)+(8*2)+(7*4)+(6*5)+(5*7)+(4*9)+(3*5)+(2*6)+(1*2)=183
183 % 10 = 3
So 1245795-62-3 is a valid CAS Registry Number.

1245795-62-3Downstream Products

1245795-62-3Relevant articles and documents

Pd-catalyzed intermolecular ortho-C-H amidation of anilides by N-nosyloxycarbamate

Ng, Ka-Ho,Chan, Albert S. C.,Yu, Wing-Yiu

supporting information; experimental part, p. 12862 - 12864 (2010/11/03)

A palladium-catalyzed ortho-C-H amidation of anilides by N-nosyloxycarbamates was developed for the synthesis of 2-aminoanilines. This reaction can be carried out under relatively mild conditions and exhibits excellent regioselectivity and functional group tolerance. The amidation reaction is probably initiated by rate-limiting C-H cyclopalladation (k H/kD = 3.7) to form an arylpalladium complex, followed by nitrene functionalization.

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