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CAS

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21639-02-1

N-p-nitrophenyloxycarbonylglycine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 21639-02-1 Structure

  • Basic information

    1. Product Name: N-p-nitrophenyloxycarbonylglycine
    2. Synonyms: N-p-nitrophenyloxycarbonylglycine
    3. CAS NO:21639-02-1
    4. Molecular Formula:
    5. Molecular Weight: 240.172
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 21639-02-1.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-p-nitrophenyloxycarbonylglycine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-p-nitrophenyloxycarbonylglycine(21639-02-1)
    11. EPA Substance Registry System: N-p-nitrophenyloxycarbonylglycine(21639-02-1)

  • 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: 21639-02-1(Hazardous Substances Data)

21639-02-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21639-02-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,6,3 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 21639-02:
(7*2)+(6*1)+(5*6)+(4*3)+(3*9)+(2*0)+(1*2)=91
91 % 10 = 1
So 21639-02-1 is a valid CAS Registry Number.

21639-02-1Relevant articles and documents

Preparation of N-acyl derivatives of amino acids from acyl chlorides and amino acids in the presence of cationic surfactants. A variation of the Schotten-Baumann method of benzoylation of amino acids

Jursic,Neumann

, p. 555 - 564 (2001)

A very efficient method for the preparation of N-acylamino acids from the corresponding acyl chloride and amino acid is described. Amino acids, potassium carbonate, acyl chloride, and a catalytic amount of cationic surfactants were mixed in tetrahydrofuran and refluxed without ever obtaining a clear reaction mixture. After hot filtration, the product was isolated from the hot tetrahydrofuran solution in very high or almost quantitative yields.

Condensation of α-Amino Acid with Amine in the Absence of a Coupling Agent

Yamaguchi, Jun-Ichi,Nagai, Shinya,Fukuoka, Emi,Suyama, Takayuki

, p. 830 - 831 (2007/10/03)

Treatment of N-(4-nitrophenoxycarbonyl)amino acid with an equimolar amount of amine in the absence of a coupling agent gave the corresponding α-amino acid amide in high yield.

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