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445231-65-2

4-phenyl-N-(1-phenylpropyl)butanamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 445231-65-2 Structure

  • Basic information

    1. Product Name: 4-phenyl-N-(1-phenylpropyl)butanamide
    2. Synonyms: 4-phenyl-N-(1-phenylpropyl)butanamide
    3. CAS NO:445231-65-2
    4. Molecular Formula: C19H23NO
    5. Molecular Weight: 281.39202
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 445231-65-2.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: 4-phenyl-N-(1-phenylpropyl)butanamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-phenyl-N-(1-phenylpropyl)butanamide(445231-65-2)
    11. EPA Substance Registry System: 4-phenyl-N-(1-phenylpropyl)butanamide(445231-65-2)

  • 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: 445231-65-2(Hazardous Substances Data)

445231-65-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 445231-65-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,5,2,3 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 445231-65:
(8*4)+(7*4)+(6*5)+(5*2)+(4*3)+(3*1)+(2*6)+(1*5)=132
132 % 10 = 2
So 445231-65-2 is a valid CAS Registry Number.

445231-65-2Downstream Products

445231-65-2Relevant articles and documents

Asymmetric direct amide synthesis by kinetic amine resolution: A chiral bifunctional aminoboronic acid catalyzed reaction between a racemic amine and an achiral carboxylic acid

Arnold, Kenny,Davies, Bryan,Hérault, Damien,Whiting, Andrew

, p. 2673 - 2676 (2008)

(Chemical Equation Presented) Let's resolve this: A planar chiral benzimidazole ferroceneboronic acid catalyst demonstrates low to moderate asymmetric induction in the kinetic resolution of racemic α-substituted benzylamines by direct amide formation with

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