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Nα-benzoyl-Nδ-cyanoornithine ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 28908-04-5 Structure
  • Basic information

    1. Product Name: Nα-benzoyl-Nδ-cyanoornithine ethyl ester
    2. Synonyms:
    3. CAS NO:28908-04-5
    4. Molecular Formula:
    5. Molecular Weight: 289.334
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 28908-04-5.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: Nα-benzoyl-Nδ-cyanoornithine ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Nα-benzoyl-Nδ-cyanoornithine ethyl ester(28908-04-5)
    11. EPA Substance Registry System: Nα-benzoyl-Nδ-cyanoornithine ethyl ester(28908-04-5)
  • 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: 28908-04-5(Hazardous Substances Data)

28908-04-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28908-04-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,9,0 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 28908-04:
(7*2)+(6*8)+(5*9)+(4*0)+(3*8)+(2*0)+(1*4)=135
135 % 10 = 5
So 28908-04-5 is a valid CAS Registry Number.

28908-04-5Relevant articles and documents

Urea cycle: Chemical simulation of arginine biosynthesis

Ranganathan,Rathi

, p. 2351 - 2354 (2007/10/02)

We have successfully simulated the salient features of the urea cycle. In this effort an appropriately protected ornithine was transformed to citrulline, via use of a novel amide transfer reagent; the citrulline, in turn, was converted into argininosuccinate which necessitated a new activation procedure to enable acceptance of dimethyl aspartate. Fragmentation of argininosuccinate under carefully controlled conditions afforded arginine. The final step in the cycle, namely, the hydrolysis of arginine to urea and ornithine, has already been accomplished. Amino group transfer from aspartate has also been demonstrated in the conversion of hypoxanthine to adenine.

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