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1203669-81-1

C53H92N6O25 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1203669-81-1 Structure

  • Basic information

    1. Product Name: C53H92N6O25
    2. Synonyms: C53H92N6O25
    3. CAS NO:1203669-81-1
    4. Molecular Formula:
    5. Molecular Weight: 1213.34
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1203669-81-1.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: C53H92N6O25(CAS DataBase Reference)
    10. NIST Chemistry Reference: C53H92N6O25(1203669-81-1)
    11. EPA Substance Registry System: C53H92N6O25(1203669-81-1)

  • 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: 1203669-81-1(Hazardous Substances Data)

1203669-81-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1203669-81-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,3,6,6 and 9 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1203669-81:
(9*1)+(8*2)+(7*0)+(6*3)+(5*6)+(4*6)+(3*9)+(2*8)+(1*1)=141
141 % 10 = 1
So 1203669-81-1 is a valid CAS Registry Number.

1203669-81-1Downstream Products

1203669-81-1Relevant articles and documents

HYDROPHOBICALLY ENHANCED AMINOGLYCOSIDES

-

, (2011/08/04)

Hydrophobically enhanced aminoglycosides have been prepared and shown to be effective antibacterial agents. These agents may be used in the treatment or prevention of various bacterial infections. Methods of preparing these agents also permit facile synth

Synthesis and antibacterial activity of amphiphilic lysine-ligated neomycin B conjugates

Bera, Smritilekha,Zhanel, George G.,Schweizer, Frank

experimental part, p. 560 - 568 (2011/05/04)

Amphiphilic lysine-ligated neomycin B building blocks were prepared by reductive amination of a protected C5″-modified neomycin B-based aldehyde and side chain-unprotected lysine or lysine-containing peptides. It was demonstrated that a suitably protected

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