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CAS

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145655-05-6

(S)-5-(Benzyl-tert-butoxycarbonyl-amino)-4-oxo-6-phenyl-hexanoic 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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  • 145655-05-6 Structure

  • Basic information

    1. Product Name: (S)-5-(Benzyl-tert-butoxycarbonyl-amino)-4-oxo-6-phenyl-hexanoic acid methyl ester
    2. Synonyms: (S)-5-(Benzyl-tert-butoxycarbonyl-amino)-4-oxo-6-phenyl-hexanoic acid methyl ester
    3. CAS NO:145655-05-6
    4. Molecular Formula:
    5. Molecular Weight: 425.525
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 145655-05-6.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)-5-(Benzyl-tert-butoxycarbonyl-amino)-4-oxo-6-phenyl-hexanoic acid methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-5-(Benzyl-tert-butoxycarbonyl-amino)-4-oxo-6-phenyl-hexanoic acid methyl ester(145655-05-6)
    11. EPA Substance Registry System: (S)-5-(Benzyl-tert-butoxycarbonyl-amino)-4-oxo-6-phenyl-hexanoic acid methyl ester(145655-05-6)

  • 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: 145655-05-6(Hazardous Substances Data)

145655-05-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 145655-05-6 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 5 respectively.
Calculate Digit Verification of CAS Registry Number 145655-05:
(8*1)+(7*4)+(6*5)+(5*6)+(4*5)+(3*5)+(2*0)+(1*5)=136
136 % 10 = 6
So 145655-05-6 is a valid CAS Registry Number.

145655-05-6Relevant 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 (2007/10/02)

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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