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1557101-65-1

N-(p-chlorocinnamoyl)-(S)-phenylalaninol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1557101-65-1 Structure

  • Basic information

    1. Product Name: N-(p-chlorocinnamoyl)-(S)-phenylalaninol
    2. Synonyms: N-(p-chlorocinnamoyl)-(S)-phenylalaninol
    3. CAS NO:1557101-65-1
    4. Molecular Formula:
    5. Molecular Weight: 315.799
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1557101-65-1.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: N-(p-chlorocinnamoyl)-(S)-phenylalaninol(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(p-chlorocinnamoyl)-(S)-phenylalaninol(1557101-65-1)
    11. EPA Substance Registry System: N-(p-chlorocinnamoyl)-(S)-phenylalaninol(1557101-65-1)

  • 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: 1557101-65-1(Hazardous Substances Data)

1557101-65-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1557101-65-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,5,7,1,0 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1557101-65:
(9*1)+(8*5)+(7*5)+(6*7)+(5*1)+(4*0)+(3*1)+(2*6)+(1*5)=151
151 % 10 = 1
So 1557101-65-1 is a valid CAS Registry Number.

1557101-65-1Relevant articles and documents

Practical and efficient synthesis of chiral 2,4-disubstituted oxazolines from β-phosphonoamides

Avalos-Alanis, Francisco G.,Hernandez-Fernandez, Eugenio,Hernandez-Romero, Rocio,Lopez-Cortina, Susana,Ordonez, Mario,Garcia-Barradas, Oscar,Lagunas-Rivera, Selene

, p. 156 - 162 (2014/02/14)

Herein we report a practical and efficient method for the synthesis of optically active 2,4-disubstituted oxazolines (S)-1a-h in good to excellent yields. The target compounds were prepared in good yield through the Horner-Wadsworth-Emmons reaction of β-phosphonoamide 3 bearing l-phenylalaninol with commercially available aryl aldehydes followed by the cyclodehydration of the corresponding N-(cinnamoyl)-(S)-phenylalaninol derivatives (S)-2a-h. Additionally, the cyclodehydration of β- phosphonoamide (S)-3 followed by the Horner-Wadsworth-Emmons reaction of β-phosphono-oxazoline (S)-4 with aryl aldehydes also gave the 2,4-disubstituted oxazolines (S)-1a-h.

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