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1442465-02-2

(S)-3-hydroxy-N-methyl-N,3-diphenylpropanamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1442465-02-2 Structure

  • Basic information

    1. Product Name: (S)-3-hydroxy-N-methyl-N,3-diphenylpropanamide
    2. Synonyms: (S)-3-hydroxy-N-methyl-N,3-diphenylpropanamide
    3. CAS NO:1442465-02-2
    4. Molecular Formula:
    5. Molecular Weight: 255.316
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1442465-02-2.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: (S)-3-hydroxy-N-methyl-N,3-diphenylpropanamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-3-hydroxy-N-methyl-N,3-diphenylpropanamide(1442465-02-2)
    11. EPA Substance Registry System: (S)-3-hydroxy-N-methyl-N,3-diphenylpropanamide(1442465-02-2)

  • 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: 1442465-02-2(Hazardous Substances Data)

1442465-02-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1442465-02-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,2,4,6 and 5 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1442465-02:
(9*1)+(8*4)+(7*4)+(6*2)+(5*4)+(4*6)+(3*5)+(2*0)+(1*2)=142
142 % 10 = 2
So 1442465-02-2 is a valid CAS Registry Number.

1442465-02-2Downstream Products

1442465-02-2Relevant articles and documents

Asymmetric β-boration of α,β-unsaturated carbonyl compounds with chiral Rh[bis(oxazolinyl)phenyl] catalysts

Toribatake, Kenji,Zhou, Li,Tsuruta, Ayae,Nishiyama, Hisao

, p. 3551 - 3560 (2013)

Chiral rhodium[bis(oxazolinyl)phenyl] complexes exhibited high catalytic activity for the β-boration of α,β-unsaturated esters, ketones, and amides with bis(pinacolato)diboron in the presence of sodium tert-butoxide to attain high enantioselectivity of up to 97%. The substrate scope and catalytic mechanism were discussed.

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