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N-(2-ethylphenyl)propanamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 91246-20-7 Structure
  • Basic information

    1. Product Name: N-(2-ethylphenyl)propanamide
    2. Synonyms: N-(2-ethylphenyl)propanamide
    3. CAS NO:91246-20-7
    4. Molecular Formula: C11H15NO
    5. Molecular Weight: 177.24
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 91246-20-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: N-(2-ethylphenyl)propanamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(2-ethylphenyl)propanamide(91246-20-7)
    11. EPA Substance Registry System: N-(2-ethylphenyl)propanamide(91246-20-7)
  • 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: 91246-20-7(Hazardous Substances Data)

91246-20-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91246-20-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,2,4 and 6 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 91246-20:
(7*9)+(6*1)+(5*2)+(4*4)+(3*6)+(2*2)+(1*0)=117
117 % 10 = 7
So 91246-20-7 is a valid CAS Registry Number.

91246-20-7Relevant articles and documents

Synthesis of Oxindole Derivatives from N-Alkenyl-o-Chloroanilides with Zero-Valent Nickel Complex

Canoira, L.,Rodriguez, J. G.

, p. 1511 - 1518 (2007/10/02)

Oxindole derivatives have been obtained from N-alkenyl-o-chloroanilides by reaction with tetrakis(triphenylphoaphine)nickel(0) in toluene as solvent in good yields.A detailed analysis of all the products of the reaction allows to confirm the postulated mechanism of the cyclization reaction.The o-chloroanilides of the 3-cyclohexenylacetic acid fails in the cyclization reaction, since the torsional hindrance seems to avoid that the endocyclic double bond may be orthogonally to the ortho-?-nickel complex intermediate on the aromatic ring.

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