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CAS

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670254-20-3

2,4-Pentadienamide, N-methyl-5-phenyl-, (2E,4E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 670254-20-3 Structure

  • Basic information

    1. Product Name: 2,4-Pentadienamide, N-methyl-5-phenyl-, (2E,4E)-
    2. Synonyms:
    3. CAS NO:670254-20-3
    4. Molecular Formula: C12H13NO
    5. Molecular Weight: 187.241
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 670254-20-3.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: 2,4-Pentadienamide, N-methyl-5-phenyl-, (2E,4E)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,4-Pentadienamide, N-methyl-5-phenyl-, (2E,4E)-(670254-20-3)
    11. EPA Substance Registry System: 2,4-Pentadienamide, N-methyl-5-phenyl-, (2E,4E)-(670254-20-3)

  • 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: 670254-20-3(Hazardous Substances Data)

670254-20-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 670254-20-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,0,2,5 and 4 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 670254-20:
(8*6)+(7*7)+(6*0)+(5*2)+(4*5)+(3*4)+(2*2)+(1*0)=143
143 % 10 = 3
So 670254-20-3 is a valid CAS Registry Number.

670254-20-3Relevant articles and documents

Efficient Synthesis of Chiral α- and β-Hydroxy Amides: Application to the Synthesis of (R)-Fluoxetine

Kakei, Hiroyuki,Nemoto, Tetsuhiro,Ohshima, Takashi,Shibasaki, Masakatsu

, p. 317 - 320 (2007/10/03)

Four flavors for epoxide openings: The regioselective openings of epoxy amides obtained by asymmetric epoxidation yields all types of aryl- and alkyl-substituted hydroxy amides sometimes counter to the reactivity of the α- and β-positions.

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