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1,3,3''-tri-N-tosylkanamycin A is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 98084-05-0 Structure
  • Basic information

    1. Product Name: 1,3,3''-tri-N-tosylkanamycin A
    2. Synonyms:
    3. CAS NO:98084-05-0
    4. Molecular Formula:
    5. Molecular Weight: 947.072
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 98084-05-0.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: 1,3,3''-tri-N-tosylkanamycin A(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,3,3''-tri-N-tosylkanamycin A(98084-05-0)
    11. EPA Substance Registry System: 1,3,3''-tri-N-tosylkanamycin A(98084-05-0)
  • 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: 98084-05-0(Hazardous Substances Data)

98084-05-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98084-05-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,0,8 and 4 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 98084-05:
(7*9)+(6*8)+(5*0)+(4*8)+(3*4)+(2*0)+(1*5)=160
160 % 10 = 0
So 98084-05-0 is a valid CAS Registry Number.

98084-05-0Relevant articles and documents

SYNTHESES OF METHYL 6-DEOXY-6-HYDROXYAMINO-α-D-GLUCOPYRANOSIDE, 6'-N-HYDROXYKANAMYCIN A, AND 6'-N-HYDROXYDIBEKACIN

Tsuchiya, Tsutomu,Nakano, Masato,Torii, Takahiro,Suzuki, Yukiko,Umezawa Sumio

, p. 195 - 206 (1985)

Methyl-6-deoxy-6-hydroxyamino-α-D-glucopyranoside has been prepared from methyl 6-amino-6-deoxy-α-D-glucopyranoside via oxidation with hydrogen peroxide in the presence of sodium tungstate , followed by reduction with sodium cyanoborohydride in an acidic medium.Acetylation of the Z isomer of 2 gave a nitrile derivative.The above oxidation-reduction procedure was applied to kanamycin A and dibekacin, starting from the corresponding 6'-amino-N-tosyl derivatives.On treatment with sodium in liquid ammonia, 6'-deamino-6'-hydroxyimino-1,3,3''-tri-N-tosylkanamycin A gave the corresponding N-detosyl derivative in good yield with the 6'-aldoxime group remaining intact, but, with 6'-deamino-6'-hydroxyimino-1,3,2',3''-tetra-N-tosyldibekacin, the N-detosyl derivative (17) was obtained only by a very short reaction period.The antibacterial activities of 17 and 6'-N-hydroxydibekacin were demonstrated.

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