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81130-91-8

1-(N-carbobenzoxy-L-alanyl)piperazine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 81130-91-8 Structure

  • Basic information

    1. Product Name: 1-(N-carbobenzoxy-L-alanyl)piperazine
    2. Synonyms:
    3. CAS NO:81130-91-8
    4. Molecular Formula:
    5. Molecular Weight: 291.35
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 81130-91-8.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: 1-(N-carbobenzoxy-L-alanyl)piperazine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(N-carbobenzoxy-L-alanyl)piperazine(81130-91-8)
    11. EPA Substance Registry System: 1-(N-carbobenzoxy-L-alanyl)piperazine(81130-91-8)

  • 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: 81130-91-8(Hazardous Substances Data)

81130-91-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81130-91-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,1,3 and 0 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 81130-91:
(7*8)+(6*1)+(5*1)+(4*3)+(3*0)+(2*9)+(1*1)=98
98 % 10 = 8
So 81130-91-8 is a valid CAS Registry Number.

81130-91-8Downstream Products

81130-91-8Relevant articles and documents

STUDIES ON THE SYNTHESIS OF CHEMOTHERAPEUTICS. PART XI. SYNTHESIS AND ANTIBACTERIAL ACTIVITIES OF PHOSPHONOPEPTIDES

Kametani, Tetsuji,Kigasawa, Kazuo,Hiiragi, Mineharu,Wakisaka, Kikuo,Haga, Seiji,et al.

, p. 1205 - 1242 (2007/10/02)

A variety of phosphonopeptides, shown in 2 as a general formula, containg natural and/or unnatural amino acids were synthesized, and their in vitro antibacterial activities were examined.N-Protected amino acids were condensed with 1-amino-ethylphosphonic acid or its ester followed by deprotection and hydrolysis to give the requisite phosphonopeptides.Several compounds showed higher levels of activity against certain members of Gram-negative bacteria than those of Alafosfalin (1) as the standard phosphonopeptide.A brief discussion on structure-activity relationships is also described.

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