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119960-02-0

methyl (R)-4-[(tert-butoxycarbonyl)amino]-3-oxopentanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 119960-02-0 Structure

  • Basic information

    1. Product Name: methyl (R)-4-[(tert-butoxycarbonyl)amino]-3-oxopentanoate
    2. Synonyms:
    3. CAS NO:119960-02-0
    4. Molecular Formula:
    5. Molecular Weight: 245.276
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 119960-02-0.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: methyl (R)-4-[(tert-butoxycarbonyl)amino]-3-oxopentanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl (R)-4-[(tert-butoxycarbonyl)amino]-3-oxopentanoate(119960-02-0)
    11. EPA Substance Registry System: methyl (R)-4-[(tert-butoxycarbonyl)amino]-3-oxopentanoate(119960-02-0)

  • 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: 119960-02-0(Hazardous Substances Data)

119960-02-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 119960-02-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,9,6 and 0 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 119960-02:
(8*1)+(7*1)+(6*9)+(5*9)+(4*6)+(3*0)+(2*0)+(1*2)=140
140 % 10 = 0
So 119960-02-0 is a valid CAS Registry Number.

119960-02-0Relevant articles and documents

α-Amino acid derived enaminones and their application in the synthesis of N-protected methyl 5-substituted-4-hydroxypyrrole-3-carboxylates and other heterocycles

Gro?elj, Uro?,?or?, Mojca,Golobi?, Amalija,Stanovnik, Branko,Svete, Jurij

, p. 11092 - 11108 (2013)

A new and simple synthesis of novel N-protected methyl 5-substituted-4- hydroxypyrrole-3-carboxylates, which exist in equilibrium with their 4-oxo tautomers, has been developed in two steps starting from N-protected α-amino acids. The key intermediates ar

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