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(E)-(S)-5-(Benzyl-tert-butoxycarbonyl-amino)-4-oxo-6-phenyl-hex-2-enoic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 145655-04-5 Structure
  • Basic information

    1. Product Name: (E)-(S)-5-(Benzyl-tert-butoxycarbonyl-amino)-4-oxo-6-phenyl-hex-2-enoic acid methyl ester
    2. Synonyms: (E)-(S)-5-(Benzyl-tert-butoxycarbonyl-amino)-4-oxo-6-phenyl-hex-2-enoic acid methyl ester
    3. CAS NO:145655-04-5
    4. Molecular Formula:
    5. Molecular Weight: 423.509
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 145655-04-5.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: (E)-(S)-5-(Benzyl-tert-butoxycarbonyl-amino)-4-oxo-6-phenyl-hex-2-enoic acid methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-(S)-5-(Benzyl-tert-butoxycarbonyl-amino)-4-oxo-6-phenyl-hex-2-enoic acid methyl ester(145655-04-5)
    11. EPA Substance Registry System: (E)-(S)-5-(Benzyl-tert-butoxycarbonyl-amino)-4-oxo-6-phenyl-hex-2-enoic acid methyl ester(145655-04-5)
  • 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: 145655-04-5(Hazardous Substances Data)

145655-04-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 145655-04-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,6,5 and 5 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 145655-04:
(8*1)+(7*4)+(6*5)+(5*6)+(4*5)+(3*5)+(2*0)+(1*4)=135
135 % 10 = 5
So 145655-04-5 is a valid CAS Registry Number.

145655-04-5Relevant articles and documents

Homologation of L-phenylalanine to ketomethylene and hydroxyethylene dipeptide isosteres via 2-thiazolyl amino ketone intermediate

Dondoni, Alessandro,Perrone, Daniela

, p. 7259 - 7262 (1992)

A highly efficient route is presented for the synthesis of N-protected isosteric dipeptides Pheψ[COCH2]Gly and Pheψ[CH(OH)CH2]Phe from L-phenylalanine through 2-thiazolyl α-amino ketone and δ-amino-γ-hydroxy-(E)-α,β-enoate derivative

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