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891699-23-3

ethyl 2-[(3R)-3-(azidomethyl)-4-benzylpiperazin-1-yl]acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 891699-23-3 Structure

  • Basic information

    1. Product Name: ethyl 2-[(3R)-3-(azidomethyl)-4-benzylpiperazin-1-yl]acetate
    2. Synonyms: ethyl 2-[(3R)-3-(azidomethyl)-4-benzylpiperazin-1-yl]acetate
    3. CAS NO:891699-23-3
    4. Molecular Formula:
    5. Molecular Weight: 317.391
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 891699-23-3.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: ethyl 2-[(3R)-3-(azidomethyl)-4-benzylpiperazin-1-yl]acetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 2-[(3R)-3-(azidomethyl)-4-benzylpiperazin-1-yl]acetate(891699-23-3)
    11. EPA Substance Registry System: ethyl 2-[(3R)-3-(azidomethyl)-4-benzylpiperazin-1-yl]acetate(891699-23-3)

  • 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: 891699-23-3(Hazardous Substances Data)

891699-23-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 891699-23-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,1,6,9 and 9 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 891699-23:
(8*8)+(7*9)+(6*1)+(5*6)+(4*9)+(3*9)+(2*2)+(1*3)=233
233 % 10 = 3
So 891699-23-3 is a valid CAS Registry Number.

891699-23-3Relevant articles and documents

Synthesis and?receptor binding studies of?3-substituted piperazine derivatives

Bedürftig, Stephan,Wünsch, Bernhard

, p. 387 - 396 (2006)

In order to find novel receptor ligands various substituents were introduced into the side chain in position 3 of the piperazine 5. During nucleophilic substitution of the hydroxy group of 5 aziridinium ions were formed, resulting in rearranged 1,4-diazep

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