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CAS

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1366297-24-6

N-(3,4-difluorophenyl)-3-hydroxypropionamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1366297-24-6 Structure

  • Basic information

    1. Product Name: N-(3,4-difluorophenyl)-3-hydroxypropionamide
    2. Synonyms:
    3. CAS NO:1366297-24-6
    4. Molecular Formula:
    5. Molecular Weight: 201.173
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1366297-24-6.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: N-(3,4-difluorophenyl)-3-hydroxypropionamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(3,4-difluorophenyl)-3-hydroxypropionamide(1366297-24-6)
    11. EPA Substance Registry System: N-(3,4-difluorophenyl)-3-hydroxypropionamide(1366297-24-6)

  • 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: 1366297-24-6(Hazardous Substances Data)

1366297-24-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1366297-24-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,6,2,9 and 7 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1366297-24:
(9*1)+(8*3)+(7*6)+(6*6)+(5*2)+(4*9)+(3*7)+(2*2)+(1*4)=186
186 % 10 = 6
So 1366297-24-6 is a valid CAS Registry Number.

1366297-24-6Upstream product

1366297-24-6Downstream Products

1366297-24-6Relevant articles and documents

Air oxidation of N-cyclopropylanilines

Blackburn, Anthony,Bowles, Daniel M.,Curran, Timothy T.,Kim, Hui

, p. 1855 - 1863 (2012/04/10)

Air oxidation of N-cyclopropylanilines was shown to occur under either ambient conditions or accelerated conditions (warming or shining light) in an open container. A subsequent fragmentation resulted in formation of the corresponding acetamide. While potential mechanisms have been previously proposed, simple aerobic oxidation to β-hydroxy-propionamides in the absence of a radical promoter has not been previously reported. Copyright Taylor & Francis Group, LLC.

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