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105469-66-7

N-(cis-β-Carboxy-acryloyl)-(L)-phenylalaninmethylester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 105469-66-7 Structure

  • Basic information

    1. Product Name: N-(cis-β-Carboxy-acryloyl)-(L)-phenylalaninmethylester
    2. Synonyms:
    3. CAS NO:105469-66-7
    4. Molecular Formula:
    5. Molecular Weight: 277.277
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 105469-66-7.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-(cis-β-Carboxy-acryloyl)-(L)-phenylalaninmethylester(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(cis-β-Carboxy-acryloyl)-(L)-phenylalaninmethylester(105469-66-7)
    11. EPA Substance Registry System: N-(cis-β-Carboxy-acryloyl)-(L)-phenylalaninmethylester(105469-66-7)

  • 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: 105469-66-7(Hazardous Substances Data)

105469-66-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105469-66-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,4,6 and 9 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 105469-66:
(8*1)+(7*0)+(6*5)+(5*4)+(4*6)+(3*9)+(2*6)+(1*6)=127
127 % 10 = 7
So 105469-66-7 is a valid CAS Registry Number.

105469-66-7Relevant articles and documents

Synthetic and NMR-Spectroscopic Investigation of Benzylamine Addition to N-Maleylamino Acid Derivatives

Griehl, Carola,Stroehl, Dieter,Jeschkeit, Hans,Kleinpeter, Erich

, p. 647 - 654 (1992)

During the addition of amines to maleylamino acids in general β-amino derivatives are formed.In order to change the reactivity within the vinylogous maleyl system we introduced the β-benzylester group into the starting compound N-(cis-β-carboxyacryloyl)-phenylalanine methylester 1.The obtained benzylester 2 is adding benzylamine in α-position yielding N-benzyl-α-aspartyl(β-benzyl)-phenylalanine methylester 4.The addition reaction was investigated by 1H-NMR-spectroscopy.The structures of the compounds have been confirmed by elemental analysis, IR, 1H-NMR and 13C-NMR spectroscopy.Keywords. α-Aspartyl peptides; N-Maleylamino acid derivatives; Nucleophilic addition.

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