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2-acetylamino-N,N-dibenzyl-4-oxo-4-phenyl-butyramide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 226985-10-0 Structure
  • Basic information

    1. Product Name: 2-acetylamino-N,N-dibenzyl-4-oxo-4-phenyl-butyramide
    2. Synonyms: 2-acetylamino-N,N-dibenzyl-4-oxo-4-phenyl-butyramide
    3. CAS NO:226985-10-0
    4. Molecular Formula:
    5. Molecular Weight: 414.504
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 226985-10-0.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-acetylamino-N,N-dibenzyl-4-oxo-4-phenyl-butyramide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-acetylamino-N,N-dibenzyl-4-oxo-4-phenyl-butyramide(226985-10-0)
    11. EPA Substance Registry System: 2-acetylamino-N,N-dibenzyl-4-oxo-4-phenyl-butyramide(226985-10-0)
  • 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: 226985-10-0(Hazardous Substances Data)

226985-10-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 226985-10-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,6,9,8 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 226985-10:
(8*2)+(7*2)+(6*6)+(5*9)+(4*8)+(3*5)+(2*1)+(1*0)=160
160 % 10 = 0
So 226985-10-0 is a valid CAS Registry Number.

226985-10-0Downstream Products

226985-10-0Relevant articles and documents

Regio- and stereoselective 1,6-photocyclization of aspartic acid- derived chiral γ-ketoamides[1]

Griesbeck, Axel G.,Heckroth, Heike,Schmickler, Hans

, p. 3137 - 3140 (2007/10/03)

Chiral α-acylamino γ-ketoamides 2 were irradiated and regioisomeric 1,6-cyclization products 3 and 4 obtained in high yields. Symmetrically N,N- disubstituted substrates 2a,b reacted diastereoselectively to give the all- cis products 3a,b in high yields. High 1,3-asymmetric induction was also observed for the unsymmetrically N,N-disubstituted 2d and 2e. The stereoselectivity of these reactions is discussed in terms of SOC-controlled spin inversion geometries.

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