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N-tert-butoxycarbonyl-4-benzyloxy-6-cyano-1-bromo-2-naphthylamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1262394-22-8 Structure
  • Basic information

    1. Product Name: N-tert-butoxycarbonyl-4-benzyloxy-6-cyano-1-bromo-2-naphthylamine
    2. Synonyms: N-tert-butoxycarbonyl-4-benzyloxy-6-cyano-1-bromo-2-naphthylamine
    3. CAS NO:1262394-22-8
    4. Molecular Formula:
    5. Molecular Weight: 453.335
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1262394-22-8.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: N-tert-butoxycarbonyl-4-benzyloxy-6-cyano-1-bromo-2-naphthylamine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-tert-butoxycarbonyl-4-benzyloxy-6-cyano-1-bromo-2-naphthylamine(1262394-22-8)
    11. EPA Substance Registry System: N-tert-butoxycarbonyl-4-benzyloxy-6-cyano-1-bromo-2-naphthylamine(1262394-22-8)
  • 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: 1262394-22-8(Hazardous Substances Data)

1262394-22-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1262394-22-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,2,3,9 and 4 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1262394-22:
(9*1)+(8*2)+(7*6)+(6*2)+(5*3)+(4*9)+(3*4)+(2*2)+(1*2)=148
148 % 10 = 8
So 1262394-22-8 is a valid CAS Registry Number.

1262394-22-8Relevant articles and documents

Synthesis of fluorescence-labelled glycosidic prodrugs based on the cytotoxic antibiotic duocarmycin

Tietze, Lutz F.,Behrendt, Frank,Major, Felix,Krewer, Birgit,Von Hof, J. Marian

supporting information; experimental part, p. 6909 - 6921 (2011/02/23)

The synthesis of the glycosidic prodrugs (1S)-30a, (1S,10R)-30b and (1S,10R)-32 labelled with different fluorescence dyes at different positions at the aromatic A-ring in 2 is described; the compounds are structurally based on the cytotoxic antibiotic duocarmycin SA. For binding, the amino compounds (1S)-3a and (1S,10R)-3b were treated with the commercially available succinimides of the dyes 5-SFX (29) and D10162 (31), respectively. Fluorescence-labelled compounds can be used for verification of interaction with cellular targets on the molecular level by use of confocal laser scanning microscopy for cell cultures and the Explore-Optics instrument (GE) for mice. The described fluorescence-labelled glycosidic prodrugs based on the cytotoxic antibiotic duocarmycine SA have high potential for selective treatment of cancer. Copyright

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