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215593-50-3

acetic acid 1-benzylcarbamoyl-2-phenylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 215593-50-3 Structure

  • Basic information

    1. Product Name: acetic acid 1-benzylcarbamoyl-2-phenylethyl ester
    2. Synonyms: acetic acid 1-benzylcarbamoyl-2-phenylethyl ester
    3. CAS NO:215593-50-3
    4. Molecular Formula:
    5. Molecular Weight: 297.354
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 215593-50-3.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: acetic acid 1-benzylcarbamoyl-2-phenylethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: acetic acid 1-benzylcarbamoyl-2-phenylethyl ester(215593-50-3)
    11. EPA Substance Registry System: acetic acid 1-benzylcarbamoyl-2-phenylethyl ester(215593-50-3)

  • 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: 215593-50-3(Hazardous Substances Data)

215593-50-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 215593-50-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,5,5,9 and 3 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 215593-50:
(8*2)+(7*1)+(6*5)+(5*5)+(4*9)+(3*3)+(2*5)+(1*0)=133
133 % 10 = 3
So 215593-50-3 is a valid CAS Registry Number.

215593-50-3Relevant articles and documents

Studies on the application of the Passerini reaction and enzymatic procedures to the synthesis of tripeptide mimetics

Szymanski, Wiktor,Zwolinska, Magdalena,Ostaszewski, Ryszard

, p. 7647 - 7653 (2007)

A new, efficient method for the multicomponent synthesis of tripeptide mimetics is presented. Simple, chemoenzymatic transformations of Passerini reaction products enable the introduction of varied amino acid moieties into the tripeptide scaffold, with co

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